Prescription and over-the-counter medication recalls
Drug recalls come from the FDA's drug enforcement reports. They range from a wrong label to a product that could be harmful, and the risk level on each notice is the FDA's own classification. Never stop a prescribed medication on the strength of a recall notice alone — the notice will say whether to return it, and your prescriber or pharmacist decides what replaces it.
4,474 stored notices, reported between Jun 20, 2012 and Sep 9, 2026. Newest first.
Reported Oct 1, 2014
Oxycodone and Acetaminophen Tablets USP 10 mg/325 mg 100 count bottles Rx Only. Manufactured by Norwich Pharmaceuticals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alvogen, Inc.
FDA (openFDA drug enforcement)
Reported Oct 1, 2014
Olanzapine Orally Disintegrating Tablets 5 mg, 30-count Bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Apotex Corp.
FDA (openFDA drug enforcement)
Reported Oct 1, 2014
Potassium Chloride Injection, 10 mEq per 100 mL, Highly Concentrated (100 mEq/L), 100 mL Sterile single dose container…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA drug enforcement)
Reported Oct 1, 2014
Buprenorphine Hydrochloride Injection, CIII, 0.3 mg base/mL ,1 mL, 10 Carpuject Sterile Cartridge Units with Luer Lock,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
FDA (openFDA drug enforcement)
Reported Oct 1, 2014
Daytrana (methylphenidate transdermal system) patch, Delivers 20 mg over 9 hours (2.2mg/hr), 1 patch per pouch ,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noven Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Oct 1, 2014
MethylPREDNISolone TABLETS, USP 4 mg, a) 100 count bottles (NDC 0603-4593-21) and b) 21 count blister pack (NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Qualitest Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
Ibuprofen Tablets, USP, 600 mg, 100 tablets per carton (10 x 10), Rx Only, Packaged and Distributed by: American Health…
High riskUsing this product could cause serious injury, illness or death — stop using it now.American Health Packaging
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
Candesartan Cilexetil and Hydrochlorothiazide Tablets 32 mg/12.5 mg, 90 count bottles, Rx only, Manufactured by: Apotex…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Apotex Corp.
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
0.9% Sodium Chloride Injection USP, packaged in a) 50 mL VIAFLEX Container bags, NDC 0338-0049-41, Product Code 2B1306;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corp.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
COUMADIN FOR INJECTION (Warfarin Sodium for Injection, USP 5 mg Single-Use Vial Rx Only Distributed by Bristol Meyers…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bristol-Meyers Squibb
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
Bupivacaine HCl Inj., USP, 0.5% (5 mg/mL), 30 mL Single-dose Preservative-Free, For Nerve Block, Caudal, and Epidural…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
THINOGENICS, WEIGHT LOSS MADE EASY! DIETARY SUPPLEMENT, 30 CAPSULES, 30 Count Bottles, THINOGENICS LLC, Nashville, TN…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nature's Universe
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, No. 158, Renmin…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nova Products, Inc.
7 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
Dermatend Original, mole, wart and skin tag remover, For external use only, Ingredient: Distilled Water, Sanguinaria…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Solace International Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
Warfarin Sodium Tablets, USP Crystalline, 2 mg, 100 and 1000 Tablet Bottles, Rx Only. Mfd. by: Taro Pharmaceutical…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Taro Pharmaceuticals U.S.A., Inc.
FDA (openFDA drug enforcement)
Reported Sep 24, 2014
NORepinephrine 4 mg in 250 mL Sodium Chloride0.9%, For IV Use Only, Flexible Bag, Rx only, UNIQUE PHARMACEUTICALS,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unique Pharmaceutical, Ltd.
FDA (openFDA drug enforcement)
Reported Sep 17, 2014
0.9% Sodium Chloride Injection, USP, 500 mL, VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA drug enforcement)
Reported Sep 17, 2014
CHIROTHIN Dietary Supplement, 2 Fl Oz (60 ml), OTC. Manufactured for ChiroNeutraceutical, 877-377-7636, Chesterfield,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.ChiroNutraceutical LLC
FDA (openFDA drug enforcement)
Reported Sep 10, 2014
Paroxetine HCL Controlled-Release Tablets 12.5 mg, 30-count bottle, Rx only, Manufactured by GlaxoSmithKline, RTP, NC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apotex Inc.
8 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 10, 2014
OXYCODONE and ACETAMINOPHEN, USP 10 mg/325 mg, CII, 100 TABLETS, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qualitest Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Sep 10, 2014
Comfort Shield Barrier Cream Cloths with dimethicone a) 8 count NDC 53462-915-80, b) 24 count NDC 53462-915-60, OTC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sage Products Inc.
FDA (openFDA drug enforcement)
Reported Sep 3, 2014
MINERAL IV Injection, compounded by Abrams Royal Pharmacy, Inc., Dallas, TX
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abrams Royal Pharamacy
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 3, 2014
VIVITROL (naltrexone for extended-release injectable suspension); 380 mg vial NDC 65757-300-01; RX Only Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alkermes, Inc.
FDA (openFDA drug enforcement)
Reported Sep 3, 2014
PEDIATRIC CARDIOPLEGIA, 255 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
High riskUsing this product could cause serious injury, illness or death — stop using it now.Central Admixture Pharmacy Services, Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.