Skin Cream - Original

Noxzema Skin Cream - Original - 14 oz. Shop In Private Skin Care Cleansers, Face Washes, Wipes, Soaps & Acne Pads Noxzema Skin Cream - Original - 14 oz. Noxzema Skin Cream - Original - 14 oz. Noxzema Skin Cream Noxzema OriginalSkin Cream For clean healthyskin, use Noxzema every time you wash. You can feel Noxzema workingas it deep cleans to remove dirt, oil and makeup without overdrying.Noxzema's formula with natural ingrients such as camphor, mentholand eucalyptus actually tingles and refreshes your skin. Beyonddaily cleansing, try Noxzema to cool and soothe overheated skin. Net Weight 14 oz.(396 g). SF118-4423 $4.99 shipping weight = (19) oz. Click here for more info about our fair shipping prices. Don't forget to check out these other versatile items: Bic Original Razors - 12 pack H127-1329 $3.99 DHS Fragrance-Free Clear Shampoo - 16 oz. H131-4384 $9.99 Gigi All Purpose Honee Wax- Microwave Formula H0365 $8.99 Lineance Leg & Body Hair Remover Kit H20404 $22.99 Lotrimin AF - Jock Itch Spray Powder M130-2827 $6.99 Nair - Cucumber Melon H130-8659 $5.99 Nair With Baby Oil - 6 oz. H194-5559 $5.99 Neutrogena Sunless Tanning Lotion - Medium SF128-0361 $9.99 Remington's Side-to-Side Nose Hair Trimmer HNE4 $13.95 embarrassing products , hardto find items , feminineneeds , men'shealth , birthcontrol , ailmentproducts , incontinence , diet products , personal hygiene , hair , skin care , home tests , gifts , ShopInPrivate Site Index, by Isdera Corp., Hazel Park, Michigan Click here to tell a friend about ShopInPrivate.com.

Body Cream Nut Butter

Amazon.com: Tree Hut Body Cream Nut Butter with Brazilian Nut and Shea Butter, 7 Ounces: Health & Personal Care Your Store Health & Personal Care See All 32 Product Categories   Your Account | Cart | Wish List | Help | Browse Brands & Products | Top Sellers | Health Care | Personal Care | Shaving & Hair Removal | Nutrition & Fitness | Baby & Child Care | Sales & Special Offers Search Amazon.com Health & Personal Care Web Search This item is not eligible for Amazon Prime, but over a million other items are. Join Amazon Prime today. Already a member? Sign in . ITEM INFORMATION Explore this item buying info label information customer reviews rate this item See more by this brand Tree Hut Customers also bought these other items... Share your thoughts write a review write a So You'd Like to... guide tell a friend about this item RATE THIS ITEM I dislike it I love it! 1 2 3 4 5 Edit your ratings Tree Hut Body Cream Nut Butter with Brazilian Nut and Shea Butter, 7 Ounces See more pictures and other information Availability: This item is currently not available. Request this item from another seller . Customers also shopped for these similar items . Features: Unique combination of Brazil Nut and Shea Nut butter combine to seal in moisture Softens dry rough skin Safe enough to use everyday Please read all label information on delivery Amazon.com Sales Rank: #4,512 in Health & Personal Care(See Top Sellers in Health & Personal Care ) Yesterday: #3,596 in Health & Personal Care Shipping: Currently, item can be shipped only within the U.S. Shipping weight: 0.44 pounds. ASIN: B0000A1VFF Item model number: 0-75371-005343 Date first available at Amazon: September 1, 2004 Expiration Dates: Amazon.com strives to provide the freshest product. If you are not satisfied with the dating on a product you receive from Amazon.com, please return it in accordance with Amazon.com's returns policy . Average Customer Review: Based on 13 reviews. Write a review . Customers who bought this itemalso bought these items: Tree Hut Body Cream - Shea Butter, 7 ounces Tree Hut Tree Hut Body Cream - Mango Butter, 7 ounces Tree Hut Tree Hut Coconut Lime Body Butter (7 Ounces) Tree Hut Tree Hut Brazilian Nut Body Lotion (8 Ounces) Tree Hut Explore Similar Items Label Information Product Description An intensive moisturizer containing Brazil Nut oil and Shea Nut butter which combine to seal in moisture and soften dry rough skin. Ingredients Water|Cyclomethicone|Glycerin|Shea Butter (butyrospermum parkii)|Glyceryl Stearate|Safflower Oil|PEG-100 Stearate|Cetearyl Alcohol|Cocoa Butter|PEG-8 Beeswax|Lanolin Alcohol|Fragrance|Brazil (bertholetta excelsa) Nut Oil|Xanthan Gum|Methylparaben|Disodium EDTA|Propylparaben|BHT|DMDM Hydantoin|Caramel Directions TO USE: Massage over the body after bathing or showering allowing the natural oils to moisturize the skin. Store in a cool place. All Customer Reviews Average Customer Review: Write an online review and share your thoughts with other customers. Search Customer Reviews mmmm , January 26, 2006 Reviewer: Jessie Schulwolf - See all my reviews this stuff is great!! the smell really does make you want to eat it....im flipping out b/c im scraping the jar as we speak! Was this review helpful to you? ( Report this ) Wonderful Moisturizer & Scent! , January 8, 2006 Reviewer: S. McBride - See all my reviews This Tree Hut Body Cream in Brazilian Nut Scent is the best I've tried & I've tried many looking for something to moisturize & soothe my dry skin. This stuff works so good-my skin is so soft! I can't stop putting it on because it smells SO GOOD!!! The scent is unbelievable, definitely one of my favorites. I also have the Coconut Lime which I enjoy too, but the Brazilian Nut is just "HEAVENLY!!" YUMMMMMM! It smells good enough to eat, although I wouldn't advise it! :) Was this review helpful to you? ( Report this ) Good Bye Dry Skin , December 28, 2005 Reviewer: Altec (Washington, DC)- See all my reviews I'm a huge fan of this cream, especially the scent. Like another review, I tried this as a less expensive alternative (on a whim) to body butter (coconut scent) by the Body Shop. It has a nutty oppose to coconut fragrance but I like both just the same. To me, they both perform the same. It's a great moisturizer after a bath or shower. I've also tried the Coconut Lime scent, which I don't like as much due to the lime overtone, but it works the same. I buy it retail around $4.99. This is a cream and thus heavier than most lotions but not greasy at all. Since I have oily skin on my face, I only use it for the body. Enjoy! Was this review helpful to you? ( Report this ) If I could give it ten stars, I would! , December 27, 2005 Reviewer: D. White (Atlanta GA)- See all my reviews THis stuff smells so good you wanna eat it! I went looking for the plain ole shea butter at Target and they were out. I found this stuff by accident. It's lovely, creamy, thick, decadent! This time of year I could start a fire, my skin is so dry. This stuff is like GOLD! Was this review helpful to you? ( Report this ) See all 13 customer reviews... Suggestion Box Your comments can help make our site better for everyone. If you've found something incorrect, broken, or frustrating on this page, let us know so that we can improve it. Please note that we are unable to respond directly to suggestions made via this form. If you need help with an order, please contact Customer Service . Please mark as many of the following boxes that apply: Product information is missing important details. Product information is incorrect. The page contains typographical errors. The page takes too long to load. The page has a software bug in it. Content violates Amazon.com's policy on offensive language . Product offered violates Amazon.com's policy on items that can be listed for sale. Comments or Examples: Examples: Missing information such as dimensions and model number, typos, inaccuracies, etc. Health & Personal Care Disclaimer: Content on this site is for reference purposes and is not intended to substitute for advice given by a physician, pharmacist, or other licensed health-care professional. You should not use this information as self-diagnosis or for treating a health problem or disease. 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Hand Care. Maintaining any

Amrep Products Overview || About Amrep || Home HAND CARE Professional maintenance does not end with abuilding, office, or plant. In some cases, it extendswell beyond the physical structure of thesefacilities. No better example of this exists thanHand Care. Maintaining any facility is an investment inimpressions. The most desirable situation is tohave this investment leave a lasting impressionof cleanliness and sanitation one that providesan experience beyond the visual sight of clean. Quality hand care products can do much morethan just provide a service to patrons. Real handcare is not simply washing your hands. Clean,enriched and moisturized hands are the result of agood hand care program. Restroom hand soaps are not all that is requiredfor complete maintenance service. Industrialapplications are very different than restroom, yetthe end result should still be the same. In order toprovide heavy duty hand care, products must beformulated with only the finest materials for removalof even the toughest dirt, grease, grime, and more.However, cleaning the most heavily soiled handsdoes not mean caring for the skin can be sacrificed.The best industrial hand care products do both. Whether you need restroom hand care, industrialhand care, or both, our Program is designed toprovide this type of cleaning and leave the properlasting impression. Dont risk missing theopportunity to make a positive impression withquality hand care. click below to jump to... Restroom Hand Soaps Industrial Hand Soaps (Water Rinsing) Industrial Hand Soaps (Waterless) Accessories Restroom Hand Soaps B00904 TROPICAL VACATION BODY WASH Formulated with gentle, biodegradable cleaners to be pH compatible with human skin, this premium total body wash for showers and hand care has a refreshing pineapple/coconut scent and luxurious emollients. Tropical Vacation is great for body, hair, face and hands and has abundant lather in hard or soft water. This thickened soap rinses easily and is appropriate for use in any stainless steel or plastic dispenser suitable for synthetic lotion soap formulas. For additional economy, Tropical Vacation may be diluted 1:1 with water. COLOR: Yellow-Green FRAGRANCE: Pineapple Coconut DILUTION: RTU pH: 7.5-8.0 USDA: n/a B00905 COCO-15 This true coconut oil based hand and body soap is a ready to useproduct fortified with glycerin emollients for the ultimate in gentleand effective skin cleaning. Ideal for those who wash frequently; it iseconomical and does not deplete natural skin oils or cause chapping.The rich opalescent color and almond fragrance make it pleasantas well as functional. COLOR: Yellow-Green FRAGRANCE: Almond DILUTION: Up to 1:3 pH: 9.0 USDA: E1 B00906 ENRICHED PINK LOTION SOAP Enriched Pink Lotion Soap is a natural soap formulated with gentle, biodegradable cleaners and skin-friendly emollients to provide mild but effective skin cleansing. This thickened pink soap has a pleasant cherry-almond fragrance and is suitable for use in all lotion dispensers. COLOR: Pink FRAGRANCE: Cherry Almond DILUTION: RTU pH: 10.0 USDA: n/a B00915 FROSTY PEARL This pearlized hand cleaner is a synthetic detergent basedbiodegradable product fortified with lanolin, moisturizers, andemollients to leave skin moist. It is excellent for removing both lightand heavy soils, greases, and other deposits without the use ofabrasives. A great all around hand soap with both a pleasantfragrance and appearance. COLOR: Salmon FRAGRANCE: Citrus DILUTION: Up to 1:4 pH: 9.5 USDA: E1 Industrial Hand Soaps (Water Rinsing) B00910 REPCO ST Our most popular heavy duty formula, this product combinespowerful industrial strength cleaning agents, detergents, andemollients to create an aggressive hand cleaner without the use ofabrasives or petroleum solvents. Ideal for daily use, it is gentle onhands and is compatible with most water types even hard water. COLOR: Yellow FRAGRANCE: Citrus DILUTION: 1:4-1:16 pH: 9.0-10.0 USDA: n/a Industrial Hand Soaps (Waterless) B00912 BRONCO Our top selling waterless formula, this traditional solvent basedproduct combines surfactant and mild solvent technology to create atruly high performance hand cleaner. It quickly and easily breaksdown dirt, grease and deposits especially around nails and cuticles.Enriched with moisturizers, it is aggressive on dirt but gentle onhands for this type of product. COLOR: Pink FRAGRANCE: Cherry DILUTION: RTU pH: 8.4 USDA: n/a B00913 MUSTANG This formula is a traditional solvent based product similar to ourB00912 but fortified with pumice abrasive particles for additionalscrubbing and abrasive power. COLOR: Green FRAGRANCE: Cherry DILUTION: RTU pH: 8.4 USDA: n/a Accessories TO1056 DISPENSER This plastic soap dispenser is a wall mount unit for use with mostwaterless formulas such as B00912 and B00913. TO1071 BRACKET This metal bracket is for the wall mounting of one gallon containersthat use traditional pumps. TO1072 PUMP This plastic pump fits most gallon containers to reliably dispensewater rinsing soaps. Products Overview || About Amrep || Home Amrep Inc. 990 Industrial Park Drive Marietta GA 30062 Toll Free 800-241-7766 770-422-2071 Fax 770-422-1737

Acne Cream (Benzoyl Peroxide

Enforcement Report for September 8, 2004 FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA Enforcement Report The FDA Enforcement Report is published weekly by the Food and Drug Administration, Department of Health and Human Services. It contains information on actions taken in connection with agency Regulatory activities. September 8, 2004 04-36 RECALLS AND FIELD CORRECTIONS: FOODS - CLASS II _______________________________ PRODUCT Assorted Old Fashioned Candies; 16 pieces per box; 7.6 oz. Recall # F-426-4. CODE All products on the market at the time the recall was initiated. RECALLING FIRM/MANUFACTURER Dulzura Borincana, Moca, PR, by store visit beginning on April 21, 2004. Firm initiated recall is complete. REASON The product contains undeclared colors - FD&C Yellow # 5, FD&C Yellow #6, and Red # 40. VOLUME OF PRODUCT IN COMMERCE 24 cases/12 bowls/16 pieces. DISTRIBUTION PR. _______________________________ PRODUCT John Frieda brand Sheer Blonde Curvaceous Blonde Curl-Defining Styler, Curls Swirls Brightens Blond Hair, packaged in 6.7 fl. Oz. plastic bottles with pump sprayer, 6 bottles per case. Item/SKU #7-17226-00502-2; Order No. 0723859. Recall # F-427-4. CODE Lots: # S001AW037 and #S001AW040. RECALLING FIRM/MANUFACTURER Andrew Jergens Co, Cincinnati, OH, by email, fax, and letter on March 22, 2004. Firm initiated recall is complete. REASON The product may be contaminated with Burkholderia cepacia. VOLUME OF PRODUCT IN COMMERCE 104 cases. DISTRIBUTION PA. RECALLS AND FIELD CORRECTIONS: FOODS - CLASS III _______________________________ PRODUCT Guava filled cakes (Panetela de Guayaba), packaged in plastic bags of 12 pieces and plastic container of 24 pieces. Recall # F-428-4. CODE All product on the market at the time the recall was initiated. RECALLING FIRM/MANUFACTURER Carlas Sweets, Bayamon, PR, by visit beginning on April 12, 2004. Firm initiated recall is ongoing. REASON Product contains undeclared color additive, FD&C Red # 40. VOLUME OF PRODUCT IN COMMERCE 8,928 units. DISTRIBUTION Local supermarkets, chain stores, and department stores. RECALLS AND FIELD CORRECTIONS: DRUGS - CLASS II _______________________________ PRODUCT a) 5% Benzoyl Peroxide Gel packaged in 1-oz. tubes, 12 per case, OTC, under the following private labels: Schnucks; 2) Harris Teeter; and 3) Finast. Recall # D-266-4; b) Invisible Acne Cream (Benzoyl Peroxide 10%), 1-oz. tubes, 12 per case, OTC, under the following private labels: 1) Western Family Maximum Strength Invisible Acne Cream; 2) Meijer Invisible Acne Cream Maximum Strength, 3) Stop & Shop Maximum Strength Invisible Acne Cream; 4) Best Yet Absolute Elements Maximum Strength Invisible Acne Cream; 5) Premier Value Maximum Strength Invisible Acne Cream; 6) Finast Maximum Strength Invisible Acne Cream; 7) Personal Expressions Vanishing Acne Cream; 8) HyVee Maximum Strength Invisible Acne Cream. Recall # D-267-4. CODE a) Lot #3J21D and 3L18D; b) Lot #3J16B, Exp. Oct 2005; 3J16C, Exp. Oct 2005; 3J16D, Exp. Oct 2005; 3K18B, Exp. Nov 2005; 4A22B, Exp. Jan 2006; 4A22C, Exp. Jan 2006; 4A28A, Exp. Jan 2006; 4B12B, Exp. Feb 2006; 4B25C, Exp. Feb 2006; 4C03C, Exp. Mar 2006; 4D03A, Exp. Apr 2006; and 4D07A, Exp. Apr 2006. RECALLING FIRM/MANUFACTURER Quailis, Inc., Des Moines, IA, by letter on July 16, 2004 and July 22, 2004. Firm initiated recall is ongoing. REASON Bacterial contamination. VOLUME OF PRODUCT IN COMMERCE 48,588 tubes. DISTRIBUTION Nationwide. RECALLS AND FIELD CORRECTIONS: DRUGS - CLASS III _______________________________ PRODUCT Prempro (conjugated estrogens/medroxyprogesterone acetate tablets) 0.45 mg/1.5 mg tablets, Rx only, 1 EZ-DIAL Dispenser of 28 tablets, NDC #0046-0937-09. Recall # D-268-4. CODE A46796, Exp. March 2005. RECALLING FIRM/MANUFACTURER Richmond Division of Wyeth, Richmond, VA, by letters dated August 12, 2004. Firm initiated recall is ongoing. REASON Dissolution Failure. VOLUME OF PRODUCT IN COMMERCE 24,871 units. DISTRIBUTION Nationwide. RECALLS AND FIELD CORRECTIONS: BIOLOGICS - CLASS II _______________________________ PRODUCT a) Whole Blood. Recall # B-1531-4; b) Red Blood Cells. Recall # B-1532-4; c) Red Blood Cells, Leukocytes Reduced. Recall # B-1533-4; d) Red Blood Cells, Leukocytes Reduced, Irradiated. Recall # B-1534-4; e) Platelets. Recall # B-1535-4; f) Platelets, Irradiated. Recall # B-1536-4; g) Fresh Frozen Plasma. Recall # B-1537-4; h) Cryoprecipitated AHF. Recall # B-1538-4. CODE a) Unit numbers: 24FC19939, 24FC19981, 24FC20405, 24FC20850, 24FC21029, 24FC21033, 24FC21035, 24FC21053, 24FC21438, 24FC21442, 24FC21456, 24FC21473; b) Unit numbers: 24FC18821, 24FC18878, 24FC18973, 24FC18974, 24FC18978, 24FC18989, 24FC19023, 24FC19039, 24FC19278, 24FC19309, 24FC19315, 24FC19380, 24FC19925, 24FC19959, 24FC19975, 24FC20016, 24FC20817, 24FC20826, 24FC20839, 24FC21037, 24FC21184, 24FC21199, 24FC21206, 24FC21301, 24FC21440, 24FC21466 c) Unit numbers: 24FC18818, 24FC18822, 24FC18824, 24FC18826, 24FC18829, 24FC18848, 24FC18852, 24FC1885 24FC18860, 24FC18864, 24FC18865, 24FC18901, 24FC18920, 24FC18923, 24FC18925, 24FC18931, 24FC18963, 24FC18972, 24FC18982, 24FC18995, 24FC18998, 24FC19005, 24FC19010, 24FC19012, 24FC19013, 24FC19289, 24FC19290, 24FC19293, 24FC19295, 24FC19296, 24FC19297, 24FC19299, 24FC19313, 24FC19314, 24FC19326, 24FC19327, 24FC19328, 24FC19330, 24FC19390, 24FC19392, 24FC19393, 24FC19394, 24FC19409, 24FC19412, 24FC19414, 24FC19930, 24FC19961, 24FC19972, 24FC19992, 24FC19993, 24FC20001, 24FC20012, 24FC20013, 24FC20014, 24FC20023, 24FC20024, 24FC20026, 24FC20028, 24FC20037, 24FC20042, 24FC20043, 24FC20044, 24FC20048, 24FC20050, 24FC20054, 24FC20067, 24FC20068, 24FC20069, 24FC20074, 24FC20075, 24FC20090, 24FC20092, 24FC20094, 24FC20096, 24FC20358, 24FC20360, 24FC20377, 24FC20378, 24FC20386, 24FC20388, 24FC20520, 24FC20539, 24FC20540, 24FC20544, 24FC20700, 24FC20735, 24FC20987, 24FC20988, 24FC21002, 24FC21003, 24FC21116, 24FC21131, 24FC21132, 24FC21133, 24FC21135, 24FC21147, 24FC21149, 24FC21183, 24FC21185, 24FC21196, 24FC21292, 24FC21300, 24FC21312, 24FC21313, 24FC21317, 24FC21322, 24FC21324, 24FC21325, 24FC21458, 24FC21474, 24FC21484, 24FC20565, 24FC20572, 24FC20574, 24FC20577, 24FC20584, 24FC20820, 24FC20829, 24FC20830, 24FC20833, 24FC20834, 24FC20837, 24FC20848, 24FC20859, 24FC20860, 24FC20861, 24KG56510, 24KG58159, 24KG58162, 24KG58163, 24KG58175, 24KG58176, 24KH95846, 24KH95847, 24KH95848, 24KH95851, 24KH95871, 24KH95875, 24KH95877, 24KH95878, 24KH95881, 24KH95882, 24KH96472, 24KJ69126, 24KJ69127, 24KJ69129, 24KJ69142, 24KJ69143, 24KJ69146, 24KJ70003, 24KJ70004, 24KJ70050, 24KJ70051, 24KJ70052, 24KJ70054, 24KJ70058, 24KJ70073, 24KJ70078, 24KJ70090, 24KJ70091, 24KJ70092, 24KJ70093, 24KJ70106, 24KJ70108, 24KJ70113, 24KJ70114, 24KJ70128, 24KJ70129, 24KJ70130, 24KJ70140, 24KJ70316, 24KJ70320, 24KJ70325, 24KJ70339, 24KJ70340, 24KJ70341, 24KJ70343, 24KJ70346, 24KJ70349, 24KJ70351, 24KJ70353, 24KM83399, 24KM83400, 24KM83406, 24KM83411, 24KM83414, 24KM83467, 24KM83469, 24KM83474, 24KM83475, 24KQ56116, 24KQ56117, 24KQ56132, 24KQ56133, 24KQ56142, 24KQ56146, 24KR21873, 24KR21874, 24KR21880, 24KR21881, 24KR21882, 24KR21884, 24KR21885, 24KR21890, 24KR21891, 24KR21892, 24KR21895, 24KR21896, 24KR21900, 24KR21902, 24KS56066, 24KS56067, 24KS56068, 24KS56071, 24KS56074, 24KS56075, 24KS56077, 24KS56078, 24KS56081 24FC18636, 24FC19021, 24FC19022, 24FC19040, 24FC19041, 24FC19051, 24FC19053, 24FC19259, 24FC19260, 24FC19261, 24FC19270, 24FC19272, 24FC19273, 24FC19345, 24FC19347, 24FC19356, 24FC19358, 24FC19360, 24FC19379, 24FC19381, 24FC19385, 24FC19731, 24FC19751, 24FC19752, 24FC19758, 24FC19767, 24FC19768, 24FC19776, 24FC19778, 24FC19779, 24FC19913, 24FC19924, 24FC19937, 24FC19944, 24FC19945, 24FC19947, 24FC19948, 24FC19956, 24FC19962, 24FC19963, 24FC20097, 24FC20149, 24FC20151, 24FC20153, 24FC20631, 24FC20635, 24FC20657, 24FC20659, 24FC20670, 24FC20672, 24FC20674, 24FC20677, 24FC20682, 24FC21021, 24FC21026, 24FC21051, 24FC21056, 24FC21057, 24KC33488, 24KC33489, 24KC33490, 24KC33492, 24KC33495, 24KC33504, 24KC33505, 24KH93842, 24KH93844, 24KH93846, 24KH93849, 24KH93851, 24KH93859, 24KH94851, 24KH94852, 24KH94853, 24KH94854, 24KH94861, 24KH95010, 24KH95450, 24KH95451, 24KH95453, 24KH95459, 24KH95467, 24KH95492, 24KH95494, 24KH95498, 24KH96442, 24KH96444, 24KJ70008, 24KJ70016, 24KJ70019, 24KJ70020, 24KJ70032, 24KJ70033, 24KJ70034, 24KJ70039, 24KJ70040, 24KJ70043, 24KJ70046, 24KJ70049, 24KL65170, 24KL65171, 24KL65173, 24KL65184, 24KL65185, 24KM83145, 24KM83148, 24KM83154, 24KM83160, 24KM83163, 24KM83164, 24KM83172, 24KQ56162, 24KQ56482, 24KQ56501; d) Unit numbers: 24FC20566, 24FC20573, 24FC19036, 24FC19037, 24FC20099, 24FC20630, 24FC20632, 24KC33486, 24KH95009, 24FC18912, 24FC18928, 24FC18983, 24FC19312, 24FC19966, 24FC20000, 24FC20045, 24FC20401, 24FC20714, 24FC21004, 24FC21118, 24FC21120, 24FC21146, 24FC21210, 24FC21461, 24FC21475; e) Unit numbers: 24FC19021, 24FC19036, 24FC19037, 24FC19050, 24FC19051, 24FC19345, 24FC19347, 24FC19379, 24FC19385, 24FC19731, 24FC19767, 24FC19768, 24FC19776, 24FC19778, 24FC19913, 24FC19924, 24FC19937, 24FC19944, 24FC19945, 24FC19947, 24FC19956, 24FC19962, 24FC20632, 24FC20657, 24FC20659, 24FC20670, 24FC20672, 24FC20674, 24FC20677, 24FC20682, 24FC21026, 24FC21051, 24FC21052, 24FC21057, 24KC33486, 24KC33489, 24KC33505, 24KH93846, 24KH93849, 24KH93851, 24KH93859, 24KH94851, 24KH94852, 24KH94861, 24KH95451, 24KH95453, 24KH95467, 24KH95494, 24KH95498, 24KH96442, 24KJ70016, 24KJ70020, 24KJ70032, 24KJ70033, 24KJ70034, 24KJ70039, 24KJ70040, 24KJ70046, 24KL65170, 24KL65173, 24KL65184, 24KL65185, 24KM83148, 24KM83154, 24KM83160, 24KM83163, 24KM83164, 24KQ56162, 24KQ56499, 24KQ56501; f) Unit numbers: 24FC19948, 24FC19963, 24KC33488, 24KC33490, 24KC33492, 24KH93842, 24KH93844, 24KH95010, 24KM83145; g) Unit numbers: 24FC19021, 24FC19024, 24FC19036, 24FC19037, 24FC19041, 24FC19050, 24FC19051, 24FC19053, 24FC19345, 24FC19347, 24FC19356, 24FC19358, 24FC19359, 24FC19360, 24FC19379, 24FC19381, 24FC19385, 24FC19731, 24FC19752, 24FC19758, 24FC19776, 24FC19778, 24FC19779, 24FC19913, 24FC19924, 24FC19937, 24FC19944, 24FC19945, 24FC19947, 24FC19948, 24FC19956, 24FC19962, 24FC19963, 24FC20151, 24FC20153, 24FC20572, 24FC20630, 24FC20632, 24FC20635, 24FC20657, 24FC20659, 24FC20670, 24FC20672, 24FC20674, 24FC20677, 24FC20682, 24FC20833, 24FC20834, 24FC20848, 24FC20859, 24FC20860, 24FC20861, 24FC21021, 24FC21026, 24FC21051, 24FC21052, 24FC21056, 24FC21057, 24FC21062, 24KC33486, 24KC33488, 24KC33489, 24KC33490, 24KC33492, 24KC33495, 24KC33505, 24KG58159, 24KG58161, 24KG58162, 24KG58163, 24KG58175, 24KG58176, 24KH93842, 24KH93844, 24KH93846, 24KH93849, 24KH93851, 24KH93859, 24KH94852, 24KH94853, 24KH94854, 24KH95010, 24KH95451, 24KH95459, 24KH95467, 24KH95494, 24KH95498, 24KH96442, 24KH96444, 24KH96472, 24KJ69126, 24KJ69127, 24KJ69142, 24KJ69143, 24KJ69146, 24KJ70078, 24KJ70129, 24KL65170, 24KL65171, 24KL65173, 24KL65184, 24KL65185, 24KM83160, 24KM83163, 24KM83164, 24KQ56162, 24KQ56499, 24KQ56501; h) Unit numbers: 24KH95875, 24KH95877, 24KH95878, 24KM83467, 24KM83474, 24KM83475. RECALLING FIRM/MANUFACTURER American Red Cross, River Valley Region, Louisville, KY, by facsimile on August 24, 2003, and by letters, dated September 3, 2003 and October 7, 2003. Firm initiated recall is complete. REASON Blood products, collected from a donor whose arm preparations were not adequately prepared, were distributed. VOLUME OF PRODUCT IN COMMERCE 589 units. DISTRIBUTION Nationwide. _______________________________ PRODUCT Source Plasma. Recall # B-1615-4. CODE Unit numbers: 7G2898, 8MW310, 8MW498, 95D691, 95D796, 95D967, 95E040, 95E289, 95E349, 95E539, 95E578, 95E716, 95F464, 9NS158, 9NS265, 9NS594, 9SW771, 9SW999, 9V5741, 9V5801, BJBZNC, BJCDLK. RECALLING FIRM/MANUFACTURER Aventis Bio-Services, Inc., Oklahoma City, OK, by facsimile dated April 20, 2001 and by email on May 16, 2003. Firm initiated recall is complete. REASON Blood products, collected from an ineligible donor who had been permanently deferred due to drug use, were distributed. VOLUME OF PRODUCT IN COMMERCE 22 units. DISTRIBUTION IL, and Germany. _______________________________ PRODUCT Red Blood Cells, Leukocytes Reduced. Recall # B-1645-4. CODE Unit number: 04KM46478. RECALLING FIRM/MANUFACTURER American Red Cross, New England Region, Dedham, MA, by letters dated April 13, 2004, and May 4, 2004. Firm initiated recall is complete. REASON Blood product, collected from an unsuitable donor based on travel to an area considered endemic for malaria, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION VT. _______________________________ PRODUCT Red Blood Cells (Apheresis), Leukoreduced. Recall # B-1764-4. CODE Units 301878101, 301878107, 301878159. RECALLING FIRM/MANUFACTURER Recalling Firm: Blood Systems Inc., Fargo, ND, by letter on December 19, 2003. Manufacturer: United Blood Services, Bismarck, ND. Firm initiated recall is complete. REASON Blood products, collected in a manner that may have compromised their sterility, were distributed. VOLUME OF PRODUCT IN COMMERCE 6 units from 3 doubles. DISTRIBUTION CA, NJ, and ND. _______________________________ PRODUCT Platelet Pheresis, Leukoreduced. Recall # B-1774-4. CODE Units: 5479032A, 5479032B, 5479032C, 5479080A, 5479080B, 5479080C. RECALLING FIRM/MANUFACTURER Coral Blood Services Inc. Bangor, ME, by telephone on May 11, 2004 and letter on May 12, 2004. Firm initiated recall is complete. REASON Blood products, collected from a donor who was taking the medication Proscar, were distributed. VOLUME OF PRODUCT IN COMMERCE 6 units. DISTRIBUTION ME. _______________________________ PRODUCT Source Plasma. Recall # B-1796-4. CODE Units DPDCDL, DPDCGV, DPDCWT, DPDDCZ, DPDDXW, DPDDRY. RECALLING FIRM/MANUFACTURER International Bio Resources, LLC, Milwaukee, WI, by facsimile dated September 25, 2002. Firm initiated recall is complete. REASON Source Plasma, collected from an ineligible donor, was distributed. VOLUME OF PRODUCT IN COMMERCE 6 units. DISTRIBUTION IL. _______________________________ PRODUCT Platelets Pheresis, Leukocytes Reduced. Recall # B-1798-4. CODE Unit number: G98916. RECALLING FIRM/MANUFACTURER Northern Illinois Blood Bank, Inc., Rockford, IL, by telephone on June 4, 2004. Firm initiated recall is complete. REASON Blood product, contaminated with coagulase-negative Staphylococcus, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION OH. _______________________________ PRODUCT a) Platelets. Recall # B-1821-4; b) Platelets, Leukocytes Removed. Recall # B-1822-4; c) Platelets, Irradiated. Recall # B-1823-4; d) Fresh Frozen Plasma. Recall # B-1824-4; e) Plasma, Frozen. Recall # B-1825-4. CODE a) Unit numbers: 49Y67247, 49F97629, 49F97919, 49S74852, 49Y46256, 49L86761, 49GF08210, 49L86831, 49G75024, 49S77099, 49S78483, 49LJ36776, 49Y66975, 49Y68019, 49LR07035, 49M29798, 49LF47660, 49S88013, and 49G97186; b) Unit numbers: 49LR25697, 49GF65893, 49M40747, 49GF66168, 49GF66163, 49GG08274, 49GG08288, 49Y83947, 49LR23218, 49LR23574, 49GG07218, 49LR26552, 49Y88280, 49M43638, and 49GG08308; c) Unit number: 49GG06960; d) Unit numbers: 49LW09875, 49LR25697, 49M40654, 49GF65893, 49M40747, 49GF65928, 49LW10123, 49GF66168, 49GF66163, 49Y86783, 49Y86768, 49GF66283, 49GG08274, 49GG08308, 49GG08288, 49GF66711, 49Y43034, 49G67557, 49GF02183, 49GF02368, 49S74472, 49GF12916, 49S77778, 49LJ36776, 49LG35118, 49GF32092, 49Y68019, 49LR05986, 49X74064, 49S88013, 49Y70271, 49GF44164, 49M33702, 49GF59138, 49GF59374, 49GG03425, 49Y83947, 49M37476, 49GF62809, 49LR23218, 49LR23574, 49M38005, 49M37999, 49M37998, 49GF64155, 49GG06960, 49S97285, 49GG07218, 49GG07494, 49GG07480, 49W37522, 49M40192, 49Y88280, 49GF68833, 49M43638, 49GF70875, 49Y89926, 49GF71467, 49GF72747, and 49GN14868; e) Unit numbers: 49LJ41837. RECALLING FIRM/MANUFACTURER American Red Cross, Southwest Region, Tulsa, OK, by telephone on April 10, 2003 and by letters dated April 16, 18, 21, and May 20, 2003, and by facsimile dated July 2, 2004. Firm initiated recall is complete. REASON Blood products, corresponding to a unit of clotted Red Blood Cells, were distributed. VOLUME OF PRODUCT IN COMMERCE 96 units. DISTRIBUTION UT, IL, OK, and TX. _______________________________ PRODUCT Source Plasma. Recall # B-1858-4. CODE Units 9NS964, 82P211, 82O863, 82O161, 82N548, 82J462, 82J334, 82J270, 82I921, 82I853, 8ZI158, 8ZH186, 8ZH080, 8ZG902, 8ZG807, 8ZG379, 8ZG293, 8ZG021, 8ZF932, 8ZE634, 8I5722, 8I5566, 8I5394, 8I5140, 8I5037, 8I4627, 8I3735, 8I3603, 8I3444, 8I2822, 8I2768, 8I2552, 8I2381, 8I2166, 8I2025, 8I1615, 8I1499, 8I1080, 71A482, 71A387, 709879, 709421, 7CY967, 7CY849, 7CY746, 6CV867, 6CV756, 6CV552, 6CU454, 6CU311, 6CU227, 6CU008, 6CT900, 6CT664, 6CT570, 6CS303, 6CR529, 6CQ220, 04L394, 04L213, 04L106, 04K740, 04K379, 04K012, 04J363, 04J165, 04J055, 04I723, 04I429, 04H960, 04H848, 04H498, 04H324, 04H196, 04G627, 04G323, 04D951, 04D774, 04D053, 04C584, 04C404, 04C326, 04C054, 04B922, 04B810, 04B691, 04B571, 04B493, 04B223, 04B170, 04A989, 04A918, 04A386, 04A140, 04A070, 038429, 038146, YFU655, YFU568, YFU336, YFU148, YFU022, YFQ795, YFQ662, YFQ439, YFQ249, YFQ048, YFT956, YFO756, YFN863, YFN721, YFM886, YFM745, YFL980, V07334, V07175, V06914, V06763, V06332, V06010, V05370, V05239, V04958, V04820, V04566, V04463, V03972, V03858, V03596, V00914, UG0107, UGZ800, UGZ578, UGZ364, UGY603, UGY517, RLS382, RLS104, RLR352, RLR151, RLQ885, RLQ566, RLQ451, RLP664, UGT030, UGS796, UGS671, UGS399, UGS232, UGS006, UGR245, UGQ309, RLP223, RLP117, RLO745, RLO595, S3P848, S3N929, S3N666, S3N371, S3N146, S3M426, S3M215, S3M018, S3L422, S3L285, S3K939, S3K134. RECALLING FIRM/MANUFACTURER Aventis Bio-Services, Inc., Oklahoma City, OK, by letters dated September 26, and September 27, 2001. Firm initiated recall is complete. REASON Source Plasma, collected from a donor who engaged in high-risk behavior, was distributed. VOLUME OF PRODUCT IN COMMERCE 168 DISTRIBUTION NC, France, and Germany. _______________________________ PRODUCT Red Blood Cells, Leukocytes Reduced. Recall # B-1860-4. CODE Unit numbers: 38H84546, 38FE77835. RECALLING FIRM/MANUFACTURER American Red Cross, Indiana-Ohio Region, Fort Wayne, IN, by telephone on April 27, 2004. Firm initiated recall is complete. REASON Blood products, collected from an unsuitable donor based on travel to an area considered endemic for malaria, were distributed. VOLUME OF PRODUCT IN COMMERCE 2 units. DISTRIBUTION IN. _______________________________ PRODUCT Red Blood Cells, Leukocytes Reduced. Recall # B-1864-4. CODE Unit 21K21241. RECALLING FIRM/MANUFACTURER American Red Cross Blood Services, Portland, OR, by telephone on May 23, 2003, and by letter dated June 2, 2003. Firm initiated recall is complete. REASON Blood product, which was collected from a donor who had an unacceptable hemoglobin at the time of donation, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION WA. _______________________________ PRODUCT Fresh Frozen Plasma. Recall # B-1865-4. CODE Unit 20GR16226. RECALLING FIRM/MANUFACTURER American Red Cross Blood Services, Boise, ID, by telephone on February 21, 2003, and by letter dated March 17, 2003. Firm initiated recall is complete. REASON Blood product, which was collected from a donor who had received the typoid vaccination, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION MT. _______________________________ PRODUCT Red Blood Cells, Leukocytes Reduced Irradiated. Recall # B-1873-4. CODE unit numbers 23149-4917 (distributed as two split units) and 23149-4931. RECALLING FIRM/MANUFACTURER Recalling Firm: Blood Systems, Inc., Scottsdale, AZ, by telephone on August 7, 2003. Manufacturer: Blood Systems, Inc., Billings, MT. Firm initiated recall is complete. REASON Blood products, for which documentation of irradiation was incomplete, were distributed. VOLUME OF PRODUCT IN COMMERCE 3 units. DISTRIBUTION MT. _______________________________ PRODUCT Platelets. Recall # B-1875-4. CODE Units 4229844, 4229846, 4229850, 4229880. RECALLING FIRM/MANUFACTURER Blood Bank of Alaska, Inc., Anchorage, AK, by letter dated December 9, 2002. Firm initiated recall is complete. REASON Blood products, which yielded a platelet count that was below the acceptable limit, were distributed. VOLUME OF PRODUCT IN COMMERCE 4 units. DISTRIBUTION AK. _______________________________ PRODUCT Red Blood Cells Frozen. Recall # B-1882-4. CODE unit 71Z69719-8 RECALLING FIRM/MANUFACTURER LifeSouth Community Blood Center, Gainesville, FL, by facsimile on December 23, 2003. Firm initiated recall is complete. REASON Blood product, which was manufactured using expired glycerol solution, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION FL. _______________________________ PRODUCT a) Red Blood Cells, Recall # B-1883-4; b) Platelets, Recall # B-1884-4; c) Fresh Frozen Plasma. Recall # B-1885-4. CODE a) Units 11GK17618 and 11GK11191; b) Unit 11GK17618; c) Units 11GK17618 and 11GK11191. RECALLING FIRM/MANUFACTURER American Red Cross Blood Services, St. Louis, MO, by telephone on April 29, 2003, or by letter dated April 28,2003. Firm initiated recall is complete. REASON Blood products, which were collected from a donor who admitted to engaging in multiple high risk behaviors, were distributed. VOLUME OF PRODUCT IN COMMERCE 5 units. DISTRIBUTION MO, and CA. _______________________________ PRODUCT Recovered Plasma. Recall # B-1886-4. CODE Unit 11GQ51677. RECALLING FIRM/MANUFACTURER American Red Cross Blood Services, St. Louis, MO, by facsimile on February 20, 2003. Firm initiated recall is complete. REASON Blood product, which was collected from a donor who was at increased risk for Creuztfeldt Jakob Disease (CJD) due to having lived in Europe between 1984 - 1987, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION Switzerland. _______________________________ PRODUCT Platelets Pheresis, Leukocytes Reduced. Recall # B-1888-4. CODE Unit number 04FP70069. RECALLING FIRM/MANUFACTURER The American National Red Cross, New England Region, Dedham, MA, by telephone on May 8, 2004, and by letter dated May 17, 2004. Firm initiated recall is complete. REASON Blood product, collected in an apheresis collection kit that had exceeded the acceptable time period for use, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION MA. _______________________________ PRODUCT a) Red Blood Cells, Leukocytes Reduced. Recall # B-1889-4; b) Platelets, Leukocytes Reduced. Recall # B-1890-4; c) Recovered Plasma. Recall # B-1891-4. CODE a), b), and c) unit number 33GE80466. RECALLING FIRM/MANUFACTURER The American National Red Cross, Connecticut Region, Farmington, CT, by facsimile on April 28, 2004, telephone on May 28, 2004, and letter on June 2, 2004. Firm initiated recall is complete. REASON Blood products collected from an unsuitable donor due to a history of travel to an area considered at increased risk of exposure to variant Creutzfeldt-Jakob Disease (vCJD). VOLUME OF PRODUCT IN COMMERCE 3 units. DISTRIBUTION CT, and CA. _______________________________ PRODUCT a) Red Blood Cells. Recall # B-1892-4; b) Fresh Frozen Plasma. Recall # B-1893-4. CODE a) and b) Unit number 4227074. RECALLING FIRM/MANUFACTURER Blood Bank of Alaska, Inc., Anchorage, AK, by letter dated November 25, 2002. Firm initiated recall is complete. REASON Blood products collected from an unsuitable donor due to a history of travel to an area considered at increased risk of exposure to variant Creutzfeldt-Jakob Disease (vCJD). VOLUME OF PRODUCT IN COMMERCE 2 units. DISTRIBUTION AK. _______________________________ PRODUCT Fresh Frozen Plasma. Recall # B-1894-4. CODE Unit number KC51510. RECALLING FIRM/MANUFACTURER HCSC Blood Center, Miller Memorial Blood Center, Bethlehem, PA, by telephone on January 23, 2004, and by letter on February 2, 2004. Firm initiated recall is complete. REASON Blood product, associated with an unit of Red Blood Cells that contained clots, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION PA. _______________________________ PRODUCT a) Red Blood Cells, Leukocytes Reduced. Recall # B-1902-4; b) Fresh Frozen Plasma. Recall # B-1903-4. CODE a) and b) Unit number 11GJ26528. RECALLING FIRM/MANUFACTURER The American National Red Cross, Missouri-Illinois Region, St. Louis, MO, by letter on February 3, 2003. Firm initiated recall is complete. REASON Blood products, that tested negative for hepatitis, but were collected from an ineligible donor due to a reported history of hepatitis, were distributed. VOLUME OF PRODUCT IN COMMERCE 2 units. DISTRIBUTION AL, and PR. _______________________________ PRODUCT a) Red Blood Cells, Leukocytes Reduced, Recall # B-1910-4; b) Red Blood Cells, Leukocytes Reduced, Irradiated. Recall # B-1911-4. CODE a) Unit 49FF51189; b) Unit 49FF50655. RECALLING FIRM/MANUFACTURER Recalling Firm: American National Red Cross, Southwest Region, Tulsa, OK, by facsimile on November 14, 2003. Manufacturing Firm: American Red Cross Blood Services, Southwest Region, College Station, TX. Firm initiated recall is complete. REASON Blood products, collected from an unsuitable donor based on travel to an area considered endemic for malaria, were distributed. VOLUME OF PRODUCT IN COMMERCE 2 units. DISTRIBUTION OK, and TX. _______________________________ PRODUCT Source Plasma. Recall # B-1916-4. CODE Units FLHSHK , FLDRWN, FLDRVJ, FLDRQG, FLDRPH , FLDRBK, FLDQLL, FLDQJX, FLDQHY , FLDQGB, FLDQDM, FLDPSC, FLDPRC, FLCPTM, FLCPRV, FLCPRC, FLCPBM, and FLCNWF. RECALLING FIRM/MANUFACTURER Aventis Bio-Services, Inc., Waco, TX, by letter dated March 21, 2003. Firm initiated recall is complete. REASON Blood products, that tested negative for viral markers, but were collected from a donor that was subsequently determined to have multiple risk factors for increased incidence of infection with human immunodeficiency virus (HIV), were distributed. VOLUME OF PRODUCT IN COMMERCE 18 units. DISTRIBUTION IL. RECALLS AND FIELD CORRECTIONS: BIOLOGICS - CLASS III _______________________________ PRODUCT Human Corneal Tissue. Recall # B-1714-4. CODE 2004-040OS, 2004-040OD. RECALLING FIRM/MANUFACTURER Great Plains Lions Eye Bank, Inc., Lubbock, TX, by letter dated June 7, 2004. Firm initiated recall is complete. REASON Human tissues for transplantation, procured from a donor whose next of kin was not asked multiple questions regarding high-risk behavior questions during the Medical/Social History Interview, were distributed. VOLUME OF PRODUCT IN COMMERCE 2 tissues. DISTRIBUTION MO. _______________________________ PRODUCT Red Blood Cells. Recall # B-1820-4. CODE Unit number: 49LF47704. RECALLING FIRM/MANUFACTURER American Red Cross, Southwest Region, Tulsa, OK, by telephone on April 10, 2003. Firm initiated recall is complete. REASON Blood products, corresponding to a unit of clotted Red Blood Cells, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION TX. _______________________________ PRODUCT a) Red Blood Cells. Recall # B-1862-4; b) Red Blood Cells Leukocytes Reduced. Recall # B-1863-4. CODE a) Unit 2421944401; b) Unit 242192958. RECALLING FIRM/MANUFACTURER Blood Systems, Inc., Rapid City, SD, by telephone on April 2, 2003. Firm initiated recall is complete. REASON Blood products, which were incorrectly tested for the presence of red cell antigens, were distributed. VOLUME OF PRODUCT IN COMMERCE 2 units. DISTRIBUTION WY. _______________________________ PRODUCT Source Plasma. Recall # B-1866-4. CODE Unit XG0013823. RECALLING FIRM/MANUFACTURER Biomat USA, Inc., Port Arthur, TX, by facsimile on April 16, 2001. Firm initiated recall is complete. REASON Blood product, which was collected from a donor whose health history screening was not adequately performed, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION KY. _______________________________ PRODUCT Source Plasma. Recall # B-1867-4. CODE Unit XN0002165. RECALLING FIRM/MANUFACTURER Biomat USA, Inc., Port Arthur, TX, by facsimile on April 16, 2001. Firm initiated recall is complete. REASON Blood product, which was collected from a donor whose health history screening was not adequately performed, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION KY. _______________________________ PRODUCT Source Plasma, Recall # B-1869-4. CODE Unit number XG0019114. RECALLING FIRM/MANUFACTURER Biomat USA, Inc., Port Arthur, TX, by facsimile on April 16, 2001. Firm initiated recall is complete. REASON Blood product, collected from a donor whose arm inspection was not documented, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION Spain. _______________________________ PRODUCT Source Plasma, Recall # B-1870-4. CODE Unit number XA0002443. RECALLING FIRM/MANUFACTURER Biomat USA, Inc., Port Arthur, TX, by facsimile on April 16, 2001. Firm initiated recall is complete. REASON Blood product, collected from a donor whose arm inspection was not documented, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION Spain. _______________________________ PRODUCT Source Plasma, Recall # B-1871-4. CODE Unit number XA0002340. RECALLING FIRM/MANUFACTURER Biomat USA, Inc., Port Arthur, TX, by facsimile on April 16, 2001. Firm initiated recall is complete. REASON Blood product, collected from a donor whose arm inspection was not documented, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION Spain. _______________________________ PRODUCT Source Plasma, Recall # B-1872-4. CODE Unit number XG0011720. RECALLING FIRM/MANUFACTURER Biomat USA, Inc., Port Arthur, TX, by facsimile on April 16, 2001. Firm initiated recall is complete. REASON Blood product, collected from a donor whose arm inspection was not documented, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION Spain. _______________________________ PRODUCT Platelets Pheresis, Leukocytes Reduced. Recall # B-1887-4. CODE Unit number 04GR22891 (distributed as two split units). RECALLING FIRM/MANUFACTURER The American National Red Cross, New England Region, Dedham, MA, by telephone on June 18, 2004, and by letter dated June 24, 2004. Firm initiated recall is complete. REASON Blood products, that were labeled leukoreduced but were not tested to determine the white blood cell count as required in the firm's standard operating procedures, were distributed. VOLUME OF PRODUCT IN COMMERCE 2 units. DISTRIBUTION MA. _______________________________ PRODUCT Platelets. Recall # B-1901-4. CODE Unit number 6034421. RECALLING FIRM/MANUFACTURER Blood Bank of Alaska, Inc., Anchorage, AK, by letter on May 28, 2003. Firm initiated recall is complete. REASON Blood product, that was not properly quarantined after the donor of the product reported a post donation illness, was distributed. VOLUME OF PRODUCT IN COMMERCE 1 unit. DISTRIBUTION MI. RECALLS AND FIELD CORRECTIONS: DEVICES - CLASS I _______________________________ PRODUCT Minerva Patient Lift, model ML-20; this lift has a passive lifting unit. Recall # Z-1381-04. CODE Model ML-20: serial numbers 952056, 952057, 952112, 952113, 952114, 952115, 952116, 952117, 962118, 952119, 952120, 952121, 962214, 962215, 962216, 962217, 962218, 962235, 962236, 962238, 962239, 962240, 962241, MPBX 97052M563, MPBX97052M564, MPBX97052M565, MPBX97052M566, MPBX97052M567, MPBX97052M568, MPBX97052M569, MPBX97052M570, MPBX97052M571, MPBX97052M572, MPBX97052M573, MPBX97052M574, MPBX97052M575, MPBX97052M576, MPBX97052M577, MPBX97052M578, MPBX97052M579, MPBX98022M649, MPBX98022M650, MPBX98022M651, MPBX98022M652, MPBX98022M653, MPBX98022M676, MPBX98022M677, MPBV00032M1013, MPBV00072M1074. RECALLING FIRM/MANUFACTURER Medibo N.V., Hanmont, Achel, Belgium, by letters dated August 6, 2004. Firm initiated recall is ongoing. REASON The hanger bar may detach from the jib yoke, the M8 bolt in the foot pedal assembly may come loose, and some units may have faulty actuator brackets on the mast assembly, resulting in the patient lift becoming unstable and allowing the patient to fall. VOLUME OF PRODUCT IN COMMERCE 64 units. DISTRIBUTION CA, FL, LA, MA, NH, NJ, NY, OH, OR and PA. RECALLS AND FIELD CORRECTIONS: DEVICES - CLASS II _______________________________ PRODUCT STS-T Mobile x-ray system used with the STS-T lithotripter. Model STS-T. Recall # Z-0884-04. CODE None provided. RECALLING FIRM/MANUFACTURER Medstone International, Inc., Aliso Viejo, CA, by letter on June 11, 2004. Firm initiated recall is complete. REASON Units are defective in that the identification and certification labels were inadequate or missing. The beam limiting device was not appropriate for general purpose radiographic procedures and the beam limiting device could ot collimate down to 125 square centimeters or less as required. VOLUME OF PRODUCT IN COMMERCE 30 units. DISTRIBUTION Nationwide. _______________________________ PRODUCT iBOT 3000 Mobility System. Independence IBOT 3000 Mobility System (Stair-climbing wheelchair), Class III restricted medical device. The device is shipped one each per wooden pallet with wooden sides and top retained by reusable bands. Recall # Z-1383-04. CODE Catalog No.s IT000101-IT000148 (inclusive), Vehicle Identification Numbers (VINs): 020404-000347, 020104-000309, 020504-000357, 021203-000308, 020204-000331, 020104-000314, 020104-000318, 021203-000301, 020304-000335, 020104-000310, 020404-000341, 021203-000299, 020204-000330, 020104-000322, 020204-000332, 020404-000350, 020404-000348, 020304-000340, 020404-000346, 020404-000342, 021203-000307, 020204-000333, 020104-000319, 021203-000304, 020404-000352, 020304-000337, 020304-000336, 020504-000356, 020404-000349, 021203-000305, 020604-000360, 020104-000317, 021203-000306, 020504-000358, 020404-000345, 020504-000354, 020304-000334, 020304-000338, 020404-000344, 020404-000351, 020504-000355, 020104-000323, 020104-000324, 021103-000291, 021203-000300, 020304-000339, 020404-000343, 020504-000359, 020604-000363, 020604-000364, 020604-000365, 020604-000366, 020604-000367, 020604-000368, 020604-000362, 021103-000290, 021103-000295, 020104-000315, 020104-000316, 020104-000320, 020104-000311, 020104-000313, 020204-000329, 020504-000353, 020104-000312, 020604-000361, 021003-000280, 020204-000328, 020104-000321, 020204-000326, 021203-000297, 021203-000298, 021203-000303, 020204-000327, 021103-000294, 021103-000286, 021103-000287, 021003-000273, 021103-000282, 021103-000292, 021103-000293, 021003-000276, 021003-000277, 021103-000285, 021103-000289, 020204-000325, 021103-000296, 021003-000278, 021003-000281, 021003-000272, 021003-000279, 021003-000274, 021003-000275, 021103-000283, 021103-000288, 021103-000284, 021203-000302. RECALLING FIRM/MANUFACTURER Independence Technology LLC, Warren, NJ, by telephone on July 2, 3, & 4, 2004 and by letters from July 5, 6, & 8, 2004. Firm initiated recall is ongoing. REASON IBOT Mobility System may tip over due to malfunction in power base. VOLUME OF PRODUCT IN COMMERCE 81 units. DISTRIBUTION Nationwide, UK, Ireland, and New Zealand. _______________________________ PRODUCT The Model 8540 Catheter Access Port Kit is intended for use in accessing the catheter via the catheter access port of Medtronic(R) implantable programmable infusion pumps (except Medtronic MiniMed pumps). The Model 8540 Catheter Access Port Kit does not have a product code for itself; it is approved under PMA P860004. PMA P860004 is classified as: pump, infusion, implanted, programmable under product code LKK. Recall # Z-1384-04. CODE CS0293. RECALLING FIRM/MANUFACTURER Medtronic Inc., Neurological & Spinal Division, Columbia Heights, MN, by letter on July 23, 2004. Firm initiated recall is ongoing. REASON The sterile tray label for the Model 8540 Catheter Access Port kit may be incorrectly labeled with a Model 8551 Refill kit label. The outer box of the affected Model 8540 Catheter Access Port kit is labeled correctly and the component parts within the sterile tray are the correct components for a Model 8540 Catheter Access Port kit. The issue is limited to one lot of product: CS0293. VOLUME OF PRODUCT IN COMMERCE 405 kits. DISTRIBUTION Nationwide and New Zealand. _______________________________ PRODUCT a) Weck Hemoclip Traditional Ligating Clips, Ref No. 523170 Hemoclip, 15 Large Tantalum Clips/Cartridge and Ref. No. 523370 Hemoclip 10 Large Tantalum Clips/Cartridge. Recall # Z-1385-04; b) Weck Atrauclip Ligating Clips, Ref. No. 121505 Atrauclip, 15 Large Titanium Clips/Cartridge and Ref. No. 121506 Atrauclip, 10 Large Titanium Clips/Cartridge. Recall # Z-1386-04; c) Weck Hemoclip Traditional Ligating Clips, Ref. No. 523770 Hemoclip, 15 Large Titanium Clips/Cartridge, and Ref. No. 523870 Hemoclip 10 Large Titanium Clips/Cartridge. Recall # Z-1387-04; d) Weck Hemoclip Traditional Ligating Clips, Ref. No. 523171 Hemoclip, 10 Large Tantalum Clips/Cartridge (Non- Sterile) and Ref. No. 523371 Hemoclip, 15 Large Tantalum Clips/Cartridge (Non-Sterile). Recall # Z-1388-04; e) Weck Hemoclip Traditional Ligating Clips, Ref. No. 523771 - Hemoclip, 15 Large Titanium Clips/Cartridge (Non-Sterile) and Ref. No. 523871- Hemoclip, 10 Large Titanium Clips/Cartridge (Non-Steile). Recall # Z-1389- 04; f) Weck Hemoclip Traditional Ligating Clips, Ref No. 523470 Hemoclip, 15 Large Stainless Steel Clips/Cartridge and Ref. No. 523670 Hemoclip, 10 Large Stainless Steel Clips/Cartridge. Recall # Z-1390-04; g) Weck Hemoclip Plus Ligating Clips, Ref. No. 533702 Hemoclip Plus, 25 Medium Titanium Clips, No Tape; Ref. No. 533737 Hemoclip Plus, 25 Small Titanium Clips/Cartridge, No Tape and Ref. No. 533872 Hemoclip Plus, 10 Large Titanium Clips/Cartridge, No Tape. Recall # Z-1391-04; h) Weck Hemoclip Plus Ligating Clips, Ref. No. 533735 and 534735 Hemoclip Plus, 25 Small Titanium Clips, Cartridge; Ref. No. 533870 Hemoclip Plus, 10 Large Titanium Clips/Cartridge and Ref. No. 533700 Hemoclip Plus, 25 Medium Titanium Clips/Cartridge. Recall # Z- 1392-04. CODE a) All lots manufactured between 2001-8 through 2002-12 for the 15 and 10 Large Tantalum Clips and additional Lots 763010, 763011, 769345 and 831864 for the 10 Large Tantalum Clips; b) All lots manufactured between 2001-8 through 2002-12; c) All lots manufactured between 2001-8 through 2002-12 for the 15 and 10 Large Titanium Clips and additional lots 799983, 816529, 826816, and 840190 for the 10 Large Titanium Clips; d) All lots manufactured between 2001-8 through 2002-12 for the 10 and 15 Large Tantalum Clips and lot 763013 for the 15 Large Tantalum Clips; e) All lots manufactured between 2001-8 throught 2002-12 for the 15 and 10 Large Titanium Clips and lots 880608 and 944135 for the 10 Large Titanium Clips; f) All lots manufactured between 2001-8 thorugh 2002-12 for 15 Large and 10 Large Stainless Steel Clips and lot 809026 for the 10 Large Stainless Steel Clips; g) All lots manufactured between 2001-8 thorugh 2002-12 for all three products and lot 763100 for 25 Medium Titanium Clips, lots 763102 and 949861 for 25 Small Clips and lot 814007 for 10 Large Titanium Clips; h) All lots manufactured between 2001-8 through 2002-12 for all three products and lots 738967, 763871 and 714124 for 25 Small Titanium Clips; lots 703251, 722666 and 825952 for 10 Large Titanium Clips and lots 738966, 754641 and 824238 for 25 Medium Titanium Clips. RECALLING FIRM/MANUFACTURER Weck, NC, by letter beginning October 24, 2003. Form initiated recall is complete. REASON Hole in the sterile unit blister pack that could compromise sterility. VOLUME OF PRODUCT IN COMMERCE 91,869 units. DISTRIBUTION Nationwide and Internationally. _______________________________ PRODUCT a) SMV FX-40 Nuclear Camera. Recall # Z-1393-04; b) SMV FX-80 Nuclear Camera. Recall # Z-1394-04. CODE a) 00000000000194, 00000000000222, 0070090040-100, 0070090040-101, 0070090040-105, 0070090040-111, 0070090040-113, 0070090040-114, 0070090040-117, 0070090040-120, 0070090040-122, 0070090040-128, 0070090040-129, 0070090040-131, 0070090040-132, 0070090040-133, 0070090040-134, 0070090040-136, 0070090040-137, 0070090040-139, 0070090040-144, 0070090040-147, 0070090040-148, 0070090040-149, 0070090040-151, 0070090040-154, 0070090040-156, 0070090040-157, 0070090040-159, 0070090040-160, 0070090040-166, 0070090040-171, 0070090040-175, 0070090040-177, 0070090040-182, 0070090040-183, 0070090040-185, 0070090040-189, 0070090040-190, 0070090040-192, 0070090040-193, 0070090040-195, 0070090040-196, 0070090040-197, 0070090040-198, 0070090040-199, 0070090040-200, 0070090040-201, 0070090040-202, 0070090040-204, 0070090040-205, 0070090040-206, 0070090040-207, 0070090040-208, 0070090040-210, 0070090040-211, 0070090040-212, 0070090040-213, 0070090040-215, 0070090040-216, 0070090040-217, 0070090040-219, 0070090040-221, 0070090040-222, 0070090040-939; b) 00000000000172, 00000000000173, 00000000000188, 00000000000203, 00000000000209, 00000000000214, 00000000000223, 0070090080-103, 0070090080-106, 0070090080-107, 0070090080-112, 0070090080-115, 0070090080-116, 0070090080-123, 0070090080-124, 0070090080-125, 0070090080-126, 0070090080-127, 0070090080-138, 0070090080-141, 0070090080-146, 0070090080-150, 0070090080-152, 0070090080-158, 0070090080-161, 0070090080-162, 0070090080-163, 0070090080-164, 0070090080-165, 0070090080-167, 0070090080-168, 0070090080-170, 0070090080-172, 0070090080-173, 0070090080-179, 0070090080-180, 0070090080-188, 0070090080-203, 0070090080-209, 0070090080-96, 0070090080-P298. RECALLING FIRM/MANUFACTURER General Electric Med Systems, Waukesha, WI, by Field Modification Instruction beginning on March 23, 2004. Firm initiated recall is ongoing. REASON The detector head of a FX-80 Nuclear camera may fall from the gantry. Three potential causes have been determined. (1) A ball nut in the detector's radial drive assembly can back out of the bearing block that contains it. (2) Misalignment of the radial drive assembly. (3) Mounting bolts on the radial drive assembly may become loose, fail, or back out. VOLUME OF PRODUCT IN COMMERCE 96 units. DISTRIBUTION Nationwide. _______________________________ PRODUCT a) Magnetom Avanto MRI System, Model 7391167. Recall # Z- 1395-04; b) Magnetom Harmony MRI System Model number 7106714. Recall # Z-1396-04; c) Magnetom Harmony MRI System Model number 5751438, Recall # Z-1397-04; d) Magnetom Symphony MRI System, Model 7106557. Recall # Z- 1398-04; e) Magnetom Symphony MRI System, Model 7104594. Recall # Z- 1399-04; f) Magnetom Sonata MRI System, Model 7388148. Recall # Z- 1400-04; g) Magnetom Sonata MRI System, Model 7104719. Recall # Z- 1401-04; h) Magnetom Sonata MRI System, Model 7106425. Recall # Z- 1402-04; i) Magnetom Trio MRI System, Model 7106441. Recall # Z- 1403-04; j) Magnetom Trio MRI System, Model 7387074. Recall # Z- 1404-4. CODE a) Serial numbers 25001 25129; b) Serial number 10502; c) Serial number 15002; d) Serial numbers 14018 and 14108; e) Serial numbers 22009, 22016, and 22081; f) Serial numbers 16502 and 16509; g) Serial numbers 21151 and 21223; h) Serial numbers 21921; i) Serial numbers 20500, 20502, and 20507; j) Serial numbers 20554, 20561, and 20569. RECALLING FIRM/MANUFACTURER Siemens Medical Solutions USA, Inc., Malvern PA, by letter on July 28, 2004. Firm initiated recall is ongoing. REASON An input error can be made with Magnetom MRI software. Software allows users to manually change Transmit Reference Voltage in certain windows. VOLUME OF PRODUCT IN COMMERCE 41 units. DISTRIBUTION Nationwide. _______________________________ PRODUCT Guardian Distal Femur Axial Pin. Recall # Z-1405-04. CODE Part No. 25002111, Serial No. 02217952 Part No. 25002112, Serial No. 01214391 Part No. 25002112, Serial No. 01215073 Part No. 25002113, Serial No. 01214533 Part No. 25002114, Serial No. 01215034 Part No. 25002114, Serial No. 01215074. RECALLING FIRM/MANUFACTURER Wright Medical Technology, Inc, Arlington, TN, by letter dated July 14, 2004. Firm initiated recall is ongoing. REASON Potential for self-locking axial pin to dislodge and back out. VOLUME OF PRODUCT IN COMMERCE 44 units. DISTRIBUTION Nationwide, Ontario, and Taiwan, ROC. _______________________________ PRODUCT a) Jackson-Pratt Hemaduct, 15 Fr round, full duct silicone wound drain; a sterile, single use only, Rx device, individually packaged, 10 drains per box, 8 boxes per case; catalog #JP-HUR880; catalog #JP-HUR880, Recall # Z-1406-04; b) Jackson-Pratt Reservoir, 400 mL suction reservoir; a sterile, single use only, Rx device used as a component of the wound drain system, individually packaged, 10 reservoirs per case, catalog #SU130-1000; Recall # Z-1407-04. CODE a) Lot 1040909; b) Lots 1040877, 1040879, 1040991, and 1040992. RECALLING FIRM/MANUFACTURER Cardinal Health, McGaw Park, IL, by telephone and letters on July 28, 2004. Firm initiated recall is ongoing. REASON The products labeled as sterile are not sterile. VOLUME OF PRODUCT IN COMMERCE 170 cases. DISTRIBUTION FL, AZ, NJ, and Canada. _______________________________ PRODUCT a) Peritoneal Lavage Kits, Model number AK-09000. Recall # Z-1408-04; b) Peritoneal Lavage Kits, Model number AK-09001. Recall # Z-1409-04. CODE a) Lot numbers: RF3111181 exp. 7/06, RF4012217 exp. 9/06, RF4012309 exp. 8/06, RF4012781 exp. 8/06, RF4023104 exp. 8/06, RF4034175 exp. 9/06, RF4034346 exp. 9/06, RF4034553 exp. 9/06, RF4055424 exp. 11/06, RF4055592 exp. 12/06, RF4055908 exp. 11/06, and RF4066874 exp. 12/06; b) Lot numbers: RF3111152 exp. 5/08, RF3121739 exp. 8/06, RF4012282 exp. 7/08, RF4012530 exp. 7/08, RF4034376 exp. 10/06, RF4034554 exp. 11/08, RF4045029 exp. 11/08, and RF4066325 exp. 1/09. RECALLING FIRM/MANUFACTURER Arrow International Inc., Reading, PA, by letter on August 9, 2004. Firm initiated recall is ongoing. REASON Wrong introducer needle in some kits. VOLUME OF PRODUCT IN COMMERCE 8,090 units. DISTRIBUTION Nationwide and Internationally. _______________________________ PRODUCT Esophageal Z-Stent Fully Coated or Uncoated Flanges, Endoprosthesis Systems with the Z Speed Introducer, Disposable - Single Use Only, Rx Only, Sterile EO, Order Number EZSP-25-10-FC. Recall # Z-1410-04. CODE Lot Number R1688574. RECALLING FIRM/MANUFACTURER Wilson-Cook Medical Inc., Winston-Salem, NC, by visit on January 30, 2003. Firm initiated recall is complete. REASON Label contains the 'Sterile EO' symbol, however the device is provided non-sterile. VOLUME OF PRODUCT IN COMMERCE 5 units. DISTRIBUTION CT, HI, LA, MO, and PA. ____________________________ PRODUCT Heat Loop cautery instrument, EO sterile - single use only; Arthrotek Ref. No. 905414 and Biomet Ref. No. 450026. Recall # Z-1411-04. CODE Arthrotek lots 049130, 300470, 278290 and 452840. Biomet lots 300450 and 228320. RECALLING FIRM/MANUFACTURER Biomet, Inc., Warsaw, IN, by letters dated July 12, and July 15, 2004. Firm initiated recall is ongoing. REASON The cautery cover cap may become dislodged during shipping or handling, the cautery switch may be activated and the cautery may melt or burn through the packaging pouch. VOLUME OF PRODUCT IN COMMERCE 130 units. DISTRIBUTION Nationwide. _______________________________ PRODUCT a) ConMed Stealth Coated Laparoscopic Electrodes with 3/32 pin (60-5158 series) as follows: Cat. #60-5158-027 Spatula 5 mm x 27 cm; Cat #60-5158-032 - Spatula 5 mm x 32 cm; Cat. #60-5158-044 - Spatula 5 mm x 44 cm; Cat #60-5158-127 - L Hook 5 mm x 27 cm; Cat #60-5158-132 - L Hook, 5 mm x 32 cm; Cat #60-5158-144 - L Hook 5 mm x 44 cm; Cat #60-5158-232 - J Hook 5mm x 32 cm; Cat. #60-5158-244 - J Hook 5mm x 44 cm; Cat #60-5158-927 - Needle 5 mm x 27 cm; Cat #60-5158-932 - Needle 5 mm x 32 cm; Recall # Z-1412-04; b) ConMed Stealth Coated Laparoscopic Electrodes with 4mm pin (60-5158 series) as follows: Cat. #60-5158-034 Spatula, 5 mm x 32 cm; Cat #60-5158-432 L Hook 5 mm x 32 cm; Cat #60-5158-934 - Needle 5mm x 32 cm. Recall # Z-1413-04. CODE a) Lot #s 0309121, 0310301, 0401051, 0404271, 0405031; Lot #s 0309011, 0309111, 0401121, 0402031, 0402271, 0404131, 0405031, 0406071; Lot #s 0309151, 0403121; Lot #s 0309021, 0309151, 0310301; Lot #s 0308071, 0308211, 0310081, 0311031, 0311101, 0401051, 0402031, 0402271, 0403121, 0404131; Lot #s 0308261, 0310061, 0310081, 0311101, 0402031, 0403031, 0403121, 0406071; Lot #s 0309121, 0310301, 0402181, 0404301; Lot #s 0309121, 0310081, 0402271, 0404301; Lot # 0309021; Lot #0308111, 0309021, 0310081, 0311101, 0401121, 0402181, 0403121; b) Lot #s 0309121; Lot #s 0308071, 0309021, 0309151, 1121; Lot #s 0309111. RECALLING FIRM/MANUFACTURER ConMed Corporation, Utica, NY, by letters dated August 9, 2004. Firm initiated recall is ongoing. REASON Insulation may pull away from the hub of the electrode exposing the conductive shaft below. This condition results in potential for electrical shock. VOLUME OF PRODUCT IN COMMERCE 6,472 units. DISTRIBUTION Nationwide and Internationally. END OF ENFORCEMENT REPORT FOR September 8, 2004 ### FDA News Page FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | Privacy | Accessibility FDA Office of Public Affairs

Microdermabrasion $34.99 List price:

Target : Artemis Woman Healing Gems Home Microdermabrasion All Products Women Men Baby Kids Home Furniture Electronics Sports Toys Music DVD Movies VHS Movies Books Shop All Departments Browse Similar Items Facial Systems Artemis Woman Spa + Relaxation Under $50 Artemis Woman Healing Gems Home Microdermabrasion $34.99 List price: $39.99 You Save: $5.00 (13%) Quantity: Sign-in for 1-Click Avg. Guest Rating: Availability : Usually ships within 1 to 2 days. • Infuses skin with pure essential oils • Exfoliates dead skin cells • Finely ground quartz crystals and natural sugar crystals • Healing Gems Facial Scrub • Exfoliating sponge, facial massager and pore cleansers Spa booked? Get radiant skin with the Artemis Woman Healing Gems Home Microdermabrasion System. This system infuses skin with pure essential oils while gently exfoliating dead skin cells with finely ground quartz crystals and natural sugar crystals. Experience the energy of amethyst spirit, balancing tourmaline, sensual rose quartz, powerful topaz and energizing clear quartz. Includes a microdermabrasion exfoliating sponge, facial massager, brush attachments, 2.5-oz. jar of Healing Crystal . . . • You may return this item to any Target store. • 2 AA batteries required • Catalog # : 694172 ASIN: B0007LQHD6 DPCI: 094-13-0139 • Imported • Shipping & Delivery Information • Estimated Ship Dimensions : 9 inches length x 7 inches width x 2 inches height • Estimated Ship weight: 0.89 pounds Better Together Buy this Artemis Woman Healing Gems Home Microdermabrasion with Artemis Woman Facial Scrub Kit today! Artemis Woman Healing Gems Home Microdermabrasion Our Price: $34.99 Artemis Woman Facial Scrub Kit Our Price: $29.99 Total List Price: $69.98 Buy Together Today: $64.98 Guest Reviews Write an online review and share your thoughts with other guests. 12 of 12 people found the following review helpful: Put on a happy face! , November 25, 2005 Reviewer: Linda O - See all my reviews I'm not usually an appliance person, but I bought this a while ago on the Target Website and I really do use it most every day. The appliance is very versatile and can be used with your favorite cleanser or with the gemstone scrub. The scrub... read complete review Was this review helpful to you? Apply for a Card Target Business Card Shipping Rates + Policies Track an Order Update an Order Return an Item Product Rebates Product Recalls Contact Us Shopping Directory More Store Locator Grocery Coupons Photo Center Portrait Studio Weekly Ad Optical Pharmacy Promotions More About Target | Careers | News | Investors | Community | Diversity | Affiliates | Team Member Services PRIVACY | Terms + Conditions California Privacy Rights ©2006 Target.com. All rights reserved. The Bullseye Design and Bullseye Dog are trademarks of Target Brands, Inc. Powered by Amazon.com