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 4, 2017
Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Oct 4, 2017
Ketorolac Trom 30 mg/mL Injection, packaged in a) 1 mL vials, NDC 61786-0741-01 (Orig: 00548-9021-00), Ref: 33631 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
FDA (openFDA drug enforcement)
Reported Oct 4, 2017
Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sandoz Inc.
FDA (openFDA drug enforcement)
Reported Oct 4, 2017
Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Sep 27, 2017
Procrit (epoetin alfa), 10,000 units/mL, packaged in a) box of 6 single use 1 mL vials (NDC 59676-310-01), b) box of 25…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amgen, Inc.
FDA (openFDA drug enforcement)
Reported Sep 27, 2017
Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-dose 100ml vial of sterile water…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Genentech, Inc.
FDA (openFDA drug enforcement)
Reported Sep 27, 2017
Aminocaproic Acid, USP (6-Aminohexanoic Acid) active pharmaceutical ingredient, packaged in a) 100 g jar (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medisca, Inc.
FDA (openFDA drug enforcement)
Reported Sep 27, 2017
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Rx Only Contains: 30 Patches…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noven Pharmaceuticals, Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 27, 2017
Quillivant XR methylphenidate HCl, for extended-release oral suspension, 600 mg/120 mL total volume (When constituted…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 27, 2017
Fentanyl Citrate (Preservative Free) 10 mcg per mL (1,000 mcg per 100 mL) 100 mL total volume in a 100 mL LifeCare Bag…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PharMedium Services, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
Phentermine, USP Capsules, 15 mg, 30 count bottles, Rx only, Packaged By: Aidarex Pharmaceuticals, Corona, CA, MFG:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aidarex Pharmaceuticals LLC
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
ANDROPHARM STEN Z (2, 17a-Dimethyl-17b-hydroxy-5a-androst-1-en-3-one 10mg and 17b-hydroxy-2a,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Andropharm, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
AMLODIPINE BESYLATE TABLET, USP, 10 mg, 1000 count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai -…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ascend Laboratories LLC
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
PF-Glutathione 200mg/ml, 30 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659 1 (877) BELLA.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bella Pharmaceuticals, Inc.
15 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
New Kopi Jantan Tradisional Natural Herbs Coffee, packaged in 13 gram red packets, and each box contains 25 packets,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bestherbs Coffee LLC
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
Ninjacof (Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz. (473 mL), Cotton Candy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Labs, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
Super Panther 7K Capsules 1250 mg blend, a) 1 count blister cards shipped in boxes of 30 (UPC# 6015577513247); and b) 6…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Chiavna Saffron LLC
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
Vitamin A&D Ointment (petroleum 93.5%), Skin Protectant, NET Wt. 0.18 OZ (5g), Manufactured for Medline Industries,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
Doctor Manzanilla Allergy & Decongestant Relief (diphenhydramine hydrochloride and phenylephrine hydrochloride) Syrup,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mid Valley Pharmaceutical
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL (Cherry Flavored), 473 mL bottles, Rx…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.VistaPharm, Inc.
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Sep 13, 2017
Povidone Iodine, USP Prep Solution, 10%, packaged in 1 gallon bottle, OTC, Manufactured for PSS World Medical, Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Degasa Sa De Cv
FDA (openFDA drug enforcement)
Reported Sep 13, 2017
Curcumin Emulsion 10mg/ml Injection, Sterile 10 mL Multiple Dose Vial, For Slow IV Administration, Compounded for a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ImprimisRx CA, Inc., dba ImprimisRx
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 13, 2017
Famotidine for Oral Suspension USP, 40 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Free recall alerts
Get alerted about new Medication recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Related categories
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.