All recall categories

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.

Drugs

Reported May 8, 2013

Pantoprazole Sodium Delayed Release Tablets USP, 40 mg, 90 count bottles, Manufactured by Jubilant Life Sciences Ltd,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Jubilant Cadista Pharmaceuticals Inc.

FDA (openFDA drug enforcement)

Drugs

Reported May 8, 2013

Daytrana (methylphenidate) transdermal system patch, Delivers 10 mg over 9 hours (1.1 mg/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)

Drugs

Reported May 8, 2013

Percocet 10/325 mg tablets, 100-count tablets per bottle, Rx only, Dist. By: Physicians Total Care, Tulsa, OK 74146;…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Physicians Total Care, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported May 8, 2013

Cherry Cepacol Sore Throat Lozenges, Benzocaine 15 mg | Menthol 3.6 mg, a)16-count, NDC 63824-711-16 b) Institutional…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Reckitt Benckiser Inc.

FDA (openFDA drug enforcement)

Drugs

Reported May 8, 2013

"Well at Wallgreens" Regular Strength Antacid Liquid (Alumina/Magnesia/Simethicone/Antacid & Anti Gas); Mint, a)12 oz…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals

FDA (openFDA drug enforcement)

Drugs

Reported May 8, 2013

Femhrt (norethindrone acetate and ethinyl estradiol) tablets, 0.5 mg/2.5 mcg, 90 count bottle (NDC#: 0430-0145-23), Rx…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Warner Chilcott Company LLC

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported May 8, 2013

Donnatal Extentabs, 0.3888mg/46.8mg, 100-count bottle (NDC # 66213-421-10), Rx only Manufactured By: West-ward…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

West-ward Pharmaceutical Corp.

FDA (openFDA drug enforcement)

Drugs

Reported May 1, 2013

TriMix Standartd (PGE Stock Sol'n) Injectable Balanced Solutions, Compounding Pharmacy a division of Axium Healthcare…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Axium Healthcare Pharmacy dba Balanced Solutions Compounding

25 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported May 1, 2013

WOW, Health Enterprises, Dietary Supplement, 30 Caplets, Distributed by: Health Enterprises, 1002 E 5th St., Canton, SD…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Brower Enterprises Inc.

FDA (openFDA drug enforcement)

Drugs

Reported May 1, 2013

Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL Single patient infusion vial, Rx only, Hospira, Inc.,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hospira Inc.

FDA (openFDA drug enforcement)

Drugs

Reported May 1, 2013

Lisinopril Tablets, USP 10 mg, Rx only, 1000 count bottles, Manufactured for: Mylan Pharmaceuticals Inc ,Morgantown, WV…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Mylan Pharmaceuticals Inc.

FDA (openFDA drug enforcement)

Drugs

Reported May 1, 2013

Pentrexcilina (acetaminophen, chlorpheniramine maleate, and phenylephrine HCl) tablets, 20-count tablets per carton,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Opmx, LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Drugs

Reported May 1, 2013

GLIMEPIRIDE TABLETS USP, 2 mg, 100-count tablets per bottle, 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)

Drugs

Reported May 1, 2013

Amoxicillin Capsules USP 500 mg, Manufactured in Austria by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540, Rx only.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sandoz Incorporated

FDA (openFDA drug enforcement)

Drugs

Reported Apr 24, 2013

buPROPion Hydrochloride Extended-Release Tablets (XL) 300 mg, 30-count tablets per bottle, Rx only, Distributed by:…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Actavis South Atlantic LLC

FDA (openFDA drug enforcement)

Drugs

Reported Apr 24, 2013

Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Body Basics Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Apr 24, 2013

Suprax (cefixime for oral suspension) USP, 100 mg/5 mL, 50 mL bottles (when reconstituted), Manufactured for Lupin…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Lupin Pharmaceuticals Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Apr 24, 2013

Levoxyl (levothyroxine sodium) tablets, USP 25 mcg, packaged in a) 100-count bottles (NDC 60793-850-01) and b)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pfizer Inc.

10 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Apr 24, 2013

Children's Acetaminophen Oral Suspension, 650 mg/20.3 mL unit dose cup (NDC 68094-650-59), packaged in 30-count cups…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Precision Dose Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Apr 24, 2013

Copaxone (glatiramer acetate injection), 20 mg/1 mL, packaged in 30 single use PRE-FILLED syringes and 33 Alcohol Preps…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teva Pharmaceuticals USA, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Apr 24, 2013

Blue Male Enhancement Pill, bulk product, by The Menz Club, Ridgeland, MS

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Menz Club, LLC

FDA (openFDA drug enforcement)

Drugs

Reported Apr 17, 2013

LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETS, USP, 20 mg/25 mg, 100 (NDC 60429-046-01) and 1,000 (NDC 60429-046-10) count…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Gsms

FDA (openFDA drug enforcement)

Drugs

Reported Apr 17, 2013

Portia (levonorgestrel and ethinyl estradiol) Tablets, USP, 0.15 mg/0.03 mg, 28-count tablets (containing 21 pink…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Teva Pharmaceuticals USA, Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Apr 10, 2013

Amoxicillin for Oral Suspension, 125mg/5mL, a) 80 mL (NDC 43598-222-80); b) 100mL, (NDC 43598-222-52); c)150 mL (NDC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dr Reddys Laboratories Tennessee LLC

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.