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 18, 2016
Paliperidone Extended-release Tablets, 1.5 mg, 30 count bottles, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mylan Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported May 18, 2016
Dryses Aluminum Chlorohydrate Antiperspirant Solution, 3.4 fl. oz (100 mL) bottle, over the counter, Manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sesderma, SL
9 more products in this recall
FDA (openFDA drug enforcement)
Reported May 11, 2016
Acetaminophen & Codeine Phosphate Tablets, 300 mg/30 mg, 15-count plastic bottle, Rx only, Mfr: Aurolife Pharma LLC,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.A-S Medication Solutions LLC.
FDA (openFDA drug enforcement)
Reported May 11, 2016
Good Neighbor Pharmacy PEG-Phen Lubricant Eye Drops (Polyethylene Glycol 400 0.4% / Propylene Glycol 0.3%), 15 ml…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn, Inc.
FDA (openFDA drug enforcement)
Reported May 11, 2016
Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-count bottle…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bryant Ranch Prepack Inc.
FDA (openFDA drug enforcement)
Reported May 11, 2016
Quelicin (Succinylcholine Chloride) Injection, USP 200 mg. (20 mg/mL), 10 mL Multiple-dose vial, packaged in 25 Unit…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hospira Inc.
FDA (openFDA drug enforcement)
Reported May 11, 2016
Oxycodone Hydrochloride Oral Solution, USP 5 mg/5 mL (1mg/ml) (NDC 66689-401-01), shrink- wrapped in 10 unit dose cups…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
FDA (openFDA drug enforcement)
Reported May 4, 2016
SKY Aspirin Chewable Tablets, 81 mg, Unit Dose 750 tablets (25 x 30) box, OTC, Distributed by: McKesson Packaging…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mckesson Packaging Services
FDA (openFDA drug enforcement)
Reported Apr 27, 2016
Zemplar (paricalcitol) capsules, 1 mcg, 30-count bottle, Rx Only, Mfd for AbbVie Inc. North Chicago, IL 60064, NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.AbbVie Inc.
FDA (openFDA drug enforcement)
Reported Apr 27, 2016
Dextrose Injection, USP, 70%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 27, 2016
Dextroamphetamine Sulfate Tablets USP, 10 mg, 100-count bottle, Rx only, Manufactured and Distributed by: Corepharma,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Impax Laboratories, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Apr 27, 2016
Telmisartan Tablets, USP, 80 mg, 30-count (3 x 10 unit-dose blisters) per carton, Rx only, Manufactured by: Torrent…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Torrent Pharmaceuticals Limited
FDA (openFDA drug enforcement)
Reported Apr 20, 2016
Fenofibrate Capsules (Micronized), 134 mg Capsules, 20-count Unit Dose Blister Packs per carton, Rx Only, Packaged and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amerisource Health Services
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Apr 20, 2016
Simvastatin Tablets, USP 5 mg Rx only, a) 90 count (NDC 24658-0300-90) and b) 1000 count (NDC 24658-0300-10 )bottles,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biocon Inc.
FDA (openFDA drug enforcement)
Reported Apr 20, 2016
Haloperidol Decanoate Injection, 50 mg/mL, 1 mL vial, Rx Only. Fresenius Kabi USA LLC, Lake Zurich, IL 60047, NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Fresenius Kabi USA, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Apr 20, 2016
Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Impax Laboratories, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Apr 13, 2016
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 10 mg,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Actavis Elizabeth LLC
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 13, 2016
Minocycline Hydrochloride Capsules USP, 100 mg*, 30 Capsules (3 x 10) Unit Dose blisters (NDC 50268-569-11, barcode…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Apace KY LLC
FDA (openFDA drug enforcement)
Reported Apr 13, 2016
Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5 mL), 16 fl oz Bottle, Rx only, Mfd For: Heritage…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bio-pharm, Inc.
FDA (openFDA drug enforcement)
Reported Apr 13, 2016
SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Jubilant Draximage Inc.
FDA (openFDA drug enforcement)
Reported Apr 13, 2016
Formula 2 (Papaverine 9 mg, Phentolamine 1 mg, Atropine 0.1 mg, PGE 10 mcg/mL) Injection, 5 mL vials, Rx only, Meditech…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meditech Laboratories, Inc.
6 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 13, 2016
Intermezzo (zolpidem tartrate) sublingual tablet 1.75 mg, CIV, 30 Ct Cartons, Rx Only. Dist by Purdue Pharma L.P.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Purdue Pharma LP
FDA (openFDA drug enforcement)
Reported Apr 13, 2016
VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing Dietary Supplement, 30-count Softgel bottles, Rx,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Virtus Pharmaceuticals, LLC
FDA (openFDA drug enforcement)
Reported Apr 6, 2016
Zoledronic Acid Injection, 5 mg/100 mL (0.05 mg/mL), 100 mL Single Use Bottle, Rx Only, Mfd. By: Gland Pharma Limited…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Reddy's Laboratories, Inc.
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.