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 Apr 5, 2017

Ciprofloxacin in Dextrose (5%) Injection, USP, 400 mg in 200 mL 5% Dextrose, Rx only, Manufactured for: Claris…

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

Claris Lifesciences Inc.

3 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Apr 5, 2017

Sensodyne Repair & Protect Whitening, (stannous fluoride 0.45% (0.15% w/v fluoride ion)), Net Wt. 3.4 oz, Distributed…

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

GSK Consumer Healthcare

FDA (openFDA drug enforcement)

Drugs

Reported Apr 5, 2017

Montelukast sodium tablets, 10 mg, 30-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc.,…

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

Hetero USA Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Apr 5, 2017

Atorvastatin Calcium Tablets, 10 mg*, 100-count Unit Dose Tablets (10 x 10) per carton, Rx only, Manufactured by: Mylan…

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

Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

FDA (openFDA drug enforcement)

Drugs

Reported Apr 5, 2017

Atorvastatin Calcium Tablets, 10 mg*, packaged in a) 90-count bottles (NDC 0378-3950-77); b) 90-count bottles (NDC…

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

Mylan Pharmaceuticals Inc.

3 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Apr 5, 2017

Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) and b) 500 count (NDC…

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

Zydus Pharmaceuticals USA Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 29, 2017

Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski,…

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

AVKARE Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 29, 2017

A+D Diaper Rash Cream with Dimethicone 1% and Zinc Oxide 10%, Packaged in a) 1.5 oz (42.5g) ( UPC 041100811288), b) 3…

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

Bayer HealthCare Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 29, 2017

Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.,…

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

Fougera Pharmaceuticals Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 29, 2017

ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati,…

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

Legacy Pharmaceutical Packaging LLC

FDA (openFDA drug enforcement)

Drugs

Reported Mar 29, 2017

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 300 mg/60 mL (25mg/5mL), Rx Only, Distributed…

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

Pfizer Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Mar 29, 2017

Testosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Only, Rx Only, Distributed by Sun…

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

Sun Pharmaceutical Industries, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 29, 2017

ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC…

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

Zydus Pharmaceuticals USA Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 22, 2017

GlipiZIDE Extended-release tablets, 2.5 mg, 30-count carton (NDC 68084-295-21), Individual dose (NDC 68084-395-11), Rx…

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

Amerisource Health Services

FDA (openFDA drug enforcement)

Drugs

Reported Mar 22, 2017

PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS Free Formula, SOOTHING MINT,…

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

Colgate Palmolive Co.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 22, 2017

Clindamycin Phosphate Topical Solution USP, 1%, packaged in a) 30 mL applicator bottles (NDC 0472-0987-91) and b) 60 mL…

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

G & W Laboratories, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 22, 2017

Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection, Preservative Free, Rx only, Compounded by Isomeric Pharmacy…

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

Isomeric Pharmacy Solution, LLC

FDA (openFDA drug enforcement)

Drugs

Reported Mar 22, 2017

PROTONIX I.V. (pantoprazole sodium) for Injection, Equivalent to 40 mg pantoprazole per vial, For I.V. infusion only,…

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

Pfizer Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 22, 2017

Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a 3 mL syringe, Local anesthetic use, Rx only,…

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

Pharmedium Services, LLC

FDA (openFDA drug enforcement)

Drugs

Reported Mar 22, 2017

Human Chorionic Gonadotropin (HCG) 5,000 units/vial and 11,000 units/vial, Rx only, Synergy RX, 4901 Morena Blvd #…

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

Synergy Rx

80 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Mar 22, 2017

Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg, 30 count HDPE bottles, Rx Only, Distributed by TEVA…

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

Teva Pharmaceuticals USA

FDA (openFDA drug enforcement)

Drugs

Reported Mar 15, 2017

Levofloxacin Ophthalmic Solution, 0.5%, Sterile, packaged in 5mL bottles, Rx Only, Manufactured by Hi-Tech Pharmacal…

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

Actavis Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 15, 2017

Edex (alprostadil for injection) 10mcg, packaged in a 2 pack carton, Rx only, Manufactured in Germany for: Actient…

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

Endo Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Mar 15, 2017

Calcipotriene Cream 0.0005%, packaged in a) 60g tube, (NDC 66993-877-61), b) 120g tube (NDC 66993-877-78), Rx Only,…

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

Leo Pharma Inc.

FDA (openFDA drug enforcement)

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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.