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 Dec 11, 2013
Badger Baby Broad Spectrum SPF 30 Zinc Oxide Sunscreen Lotion Chamomile & Calendula, 4fFl.oz Tube, UPC code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W.S. Badger Company Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY ACTAVIS ELIZABETH LLC.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Actavis Elizabeth LLC
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
Acyclovir Tablets USP 800 mg ,(NDC 60505-5307-1), Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada M9L…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apotex Inc.
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
Cetacaine Liquid Topical Anesthetic, Rx Only, a) 14 g bottle (NDC 10223-0202-2); Kit w/14 g (NDC 10223-0202-3); 30 g…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cetylite Industries, Inc.
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
PACLITAXEL INJECTION, USP (semisynthetic); 300 mg/50 mL; (6 mg/mL); Multiple Dose Vial;(NDC 63323-763-50); Rx Only;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Fresenius Kabi USA, LLC
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
J.R. Jack Rabbit All Natural Herbal Supplement, One tablet can last 24-72 hours, 4-count tablets per blister pack,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jack Rabbit, Inc.
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
Loratadine, USP 10 mg, Antihistamine, packaged in blister packs. All manufactured by Novartis Consumer Health, Inc,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
Acanya (Clindamycin Phosphate and Benzoyl Peroxide) Gel 1.2% and 2.5%, Net Wt. 3.5 g, Rx Only, Sample - not for sale,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Valeant Pharmaceuticals North Am
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Affirm XL Nutritional Supplement, 1 and 10 count blister packs and single pill packs, Manufactured by Dongseo Biopharm…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Affirm XL, Inc.
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Oxcarbazepine Oral Suspension, 300 mg/5 mL, 250 mL bottle, Rx only, Boehringer Ingelheim, Roxane Laboratories, Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boehringer Ingelheim Roxane Inc.
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Spironolactone tablets, USP 25 mg, Rx only, 500 count bottle, Distributed By: Greenstone LLC, Peapack, NJ 07977, NDC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greenstone LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil (Scalp Oil), 118.28 mL (4 Fl. oz.) bottle, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hill Dermaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Omeprazole Delayed-Release Capsules, USP, 20 mg, Rx Only, 1000 Capsules per bottle, Distributed by: Kremers Urban…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kremers Urban Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Acetaminophen suspension liquid, 160 mg/5 mL, dye-free cherry flavor, co-packaged with an oral dosing syringe in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.L. Perrigo Co.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Aldactone (spironolactone) tablets, USP, 100 mg, 100-count bottles, Rx only, Distributed by G.D. Searle, Division of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer US Pharmaceutical Group
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Copaxone (glatiramer acetate injection), 20 mg/1 mL, 1 mL pre-filled syringe, packaged in 30 single-use PRE-FILLED…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Nov 13, 2013
Prolia (denosumab) Injection, 60 mg/mL, 1 x 60 mg Single Use Prefilled Syringe per carton, Rx only, Manufactured by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amgen, Inc.
FDA (openFDA drug enforcement)
Reported Nov 13, 2013
Extended Phenytoin Sodium Capsules, USP, 100 mg, 1000 CAPSULES, Rx only, amneal PHARMACEUTICALS label, NDC 65162-212-11…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amneal Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Nov 13, 2013
Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL single patient infusion vial packaged in 5 Units x 20…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
FDA (openFDA drug enforcement)
Reported Nov 13, 2013
Amlodipine Besylate Tablets, USP, 2.5 mg, packaged in a) 90-count bottles (NDC 0378-5208-77) and b) 500-count bottles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mylan Pharmaceuticals Inc.
11 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 13, 2013
Ropinirole, extended-release tablets, 2 mg, 90 count bottle, Rx only, Manufactured in India by Sandoz Private Ltd, for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz, Inc.
FDA (openFDA drug enforcement)
Reported Nov 13, 2013
Irinotecan Hydrochloride Injection, 40 mg/2 mL (20 mg/mL), 1 x 2 mL Single Dose Vial per carton, Rx only, Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.West-Ward Pharmaceutical Corp.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 6, 2013
Bevacizumab 25mg/mL, prepared as pre-filled syringes in 0.05 mL and 0.06 mL sizes, Fallon Wellness Pharmacy, Latham, NY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fallon Wellness Pharmacy LLC
FDA (openFDA drug enforcement)
Reported Oct 30, 2013
GILTUSS ANTITUSSIVE EXPECTORANT AND NASAL DECONGESTANT, 1 fl. oz. (NDC 58552-122-01) and 8 fl. oz. (NDC 58552-122-08),…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hi-Tech Pharmacal Co., 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.