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 May 22, 2019
Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.D.B.P. Distribution
FDA (openFDA drug enforcement)
Reported May 22, 2019
Relpax (eletriptan HBr) 40 mg, a) 12 tablets 2 cards x six 40 mg tablets per blister pack, NDC 0049-2340-05; b) 6…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported May 22, 2019
Losartan Potassium Tab. USP 50mg, a) 30 count bottle (NDC 68788-0048-03) and b) 90 count bottle (NDC 68788-0048-09), Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported May 22, 2019
CVS Health Children's Pain & Fever Acetaminophen 160 mg/5 mL Pain reliever/Fever reducer Single-Use Vials Cherry Flavor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unipharma, Llc.
10 more products in this recall
FDA (openFDA drug enforcement)
Reported May 15, 2019
FENTANYL Transdermal System, 12 mcg/h, five (12 mcg/h) systems per carton, Rx only, Distributed by: Alvogen, Inc., Pine…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alvogen, Inc.
FDA (openFDA drug enforcement)
Reported May 15, 2019
Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Par Pharmaceutical, Inc.
FDA (openFDA drug enforcement)
Reported May 15, 2019
Ketorolac Tromethamine Injection, USP, 60 mg per 2 mL (30 mg per mL), 2 mL Vials, Rx only, Mfd. for Sagent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sagent Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported May 15, 2019
Acyclovir Tablets, USP, 400 mg, 100 count bottles, Rx Only Manufactured by: Cadila Healthcare Ltd., India Distributed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals USA Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 8, 2019
HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Pharma Inc.
FDA (openFDA drug enforcement)
Reported May 8, 2019
Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters, 20%, 0.5%, Net WT 2.75 oz (78g);…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Advantice Health
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 8, 2019
GlipiZIDE Extended-release Tablets, 2.5 mg, 30 Tablets (3 x 10), Rx Only, Packaged and Distributed by: American Health…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Health Packaging
FDA (openFDA drug enforcement)
Reported May 8, 2019
Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Dose Rx Only NDC 50268-517-15 Manufactured for: AvKARE Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AVKARE Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 8, 2019
BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV INJ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Customceutical Compounding
9 more products in this recall
FDA (openFDA drug enforcement)
Reported May 8, 2019
Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distributed by: The Kroger Co, Cincinnati, OH…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Legacy Pharmaceutical Packaging LLC
FDA (openFDA drug enforcement)
Reported May 8, 2019
BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This biologic product was repackaged by AmEx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacifico National, Inc. dba AmEx Pharmacy
FDA (openFDA drug enforcement)
Reported May 8, 2019
Losartan Potassium/HCTZ, 100 mg/12.5 mg Tablet, 90-Count bottle, Manufactured by Torrent Pharmaceuticals, Distributed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
FDA (openFDA drug enforcement)
Reported May 8, 2019
Losartan Potassium Tablets, USP, 25 mg, a) 90-count (NDC: 13668-113-90), b)1000-count (NDC: 13668-113-10) per bottle,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported May 8, 2019
Revonto (dantrolene sodium for injection), 20 mg/vial, For treatment of malignant hyperthermia, For Intravenous Use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Worldmeds LLC
FDA (openFDA drug enforcement)
Reported May 1, 2019
Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 25 Ampules per carton, (2 mL each), Rx only, Manufactured…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Akorn Inc.
FDA (openFDA drug enforcement)
Reported May 1, 2019
Dexmedetomidine 400 mcg in NS 100 mL bag, Made by: Enterprise Pharmacy, 4400 Golf Acres Drive, Bldg. J Suite E,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CMC Enterprise Pharmacy
31 more products in this recall
FDA (openFDA drug enforcement)
Reported May 1, 2019
Morphine Sulfate Extended-Release Tablets, 15 mg, 100-count bottles, Rx Only, Manufactured by: Novel Laboratories, Inc.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Somerset
4 more products in this recall
FDA (openFDA drug enforcement)
Reported May 1, 2019
Carvedilol Tablets, USP, 3.125 mg, 500-count bottle, Rx Only, Manufactured by: Cadila Healthcare Ltd., India;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Zydus Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Apr 24, 2019
Acetylcysteine 10% Ophthalmic Eye Drop 2 mL droptainer, Anderson Compounding Pharmacy 310 Bluff City Hwy Bristol, TN.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Anderson Compounding Pharmacy, Inc. dba Anderson Compounding Pharmacy
67 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 24, 2019
Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Brian P. Richardson
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.