Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
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Other Drugs
💊 Drugs • 3,200 recalls
Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Class I - Dangerous
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Class I - Dangerous
Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner. The available iodine in the product is less than as stated on the product label.
Class I - Dangerous
Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner. The available iodine in the product is less than as stated on the product label.
ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY
Teva Pharmaceuticals USA
Class I - Dangerous
Non-sterility: due to a failed sterility test
SEXY MONKEY, 2000 mg, 1 count blister, Distributed by A Herbal Bio, Inc., Bayside, NY.
Schindele Enterprises
Class I - Dangerous
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Red Yeast Rice High Potency Dietary Supplement, 600 mg, packaged in a) 120-count VegeCaps per bottle (UPC 8 01650 02205 9) and b) 500-count VegeCaps per bottle (UPC 8 01650 02206 6), Manufactured by: Back to Health, Eugene, Oregon 97402.
Independent Nutrition Center
Class I - Dangerous
Marketed Without An Approved NDA/ANDA: Product is being recalled due to excessive levels of lovastatin. Lovastatin is an FDA approved drug making this dietary supplement an unapproved new drug.
XZEN PLATINUM, 750 mg, Distributed by: XZEN, Los Angeles, CA.
Schindele Enterprises
Class I - Dangerous
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Magic For Men, packaged in 1ct blister pack and 12-pill/bottle, 390 mg Manufactured For: BTQ Ski, Inc., Chicago, IL 60638
Schindele Enterprises
Class I - Dangerous
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Class I - Dangerous
Marketed Without an Approved NDA/ANDA: Products found to contain undeclared sibutramine, N-Desmethylsibutramine, and N-di- Desmethylsibutramine. Sibutramine was removed from the U.S. market for safety reasons, making these products unapproved new drugs.
Class I - Dangerous
Defective Delivery System; defective valve
Class I - Dangerous
First Aid Only, Inc is recalling Smart Tab First Aid ezRefill System Ibuprofen boxes and First Aid Cabinets containing these Ibuprofen boxes. Ibuprofen boxes (FAE 7014) were accidentally used to package aspirin packs (10 packs of 2 / 235mg tablets).