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 12, 2016
PredniSONE Tablets USP, 1 mg, 100-count bottles, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.West-Ward Pharmaceutical
FDA (openFDA drug enforcement)
Reported Oct 5, 2016
Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mckesson Packaging Services
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 5, 2016
PREMARIN (conjugated estrogen tablets, USP) 1.25 mg, 1000- count bottle, Rx only, Distributed by: Wyeth Pharmaceuticals…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Oct 5, 2016
Chlorpheniramine Maleate 10 mg/ml, 30 ml MDV, Rx, Vital Care Compounder, Hattiesburg, MS 39402
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmacy Plus, Inc. dba Vital Care Compounder
20 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 5, 2016
Sennazon (sennosides) Syrup, 8.8 mg, 8 fl. oz. (237 mL) bottle, Mfd. for: Bayshore Pharmaceuticals, Tampla, FL 33619,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmatech LLC
6 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 5, 2016
Lamotrigine Tablets, USP, 150 mg, 500-count Tablets per bottle, Rx only, Manufactured by: Unichem Laboratories LTD.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Unichem Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Sep 28, 2016
Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial, Rx Only, For Subcutaneous Injection only, Manufactured…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Genzyme Corporation / Genzyme Biosurgery
FDA (openFDA drug enforcement)
Reported Sep 28, 2016
Escitalopram Tablets USP 20 mg, 100-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Baltimore, MD,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Limited
FDA (openFDA drug enforcement)
Reported Sep 28, 2016
Lisinopril Tablets USP, 30 mg, packaged in a) 500-count bottles (NDC 68180-516-02) and b) 100-count bottles (NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Pharmaceuticals Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 28, 2016
Mucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser, Parsippany, NJ 07054-0224 UPC 363824951737 NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Reckitt Benckiser LLC
FDA (openFDA drug enforcement)
Reported Sep 28, 2016
Ephedrine Sulfate Injection, USP, 50 mg/mL, 1 mL Fill in a 2mL Vial (NDC 66758-008-01), packaged in 25 x 2 mL Vials per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 28, 2016
Carvediol Tablets , USP, 3.125 mg, 100-count bottle (NDC 57664-242-88). 500-count bottle (NDC 57664-242-13), 1000-count…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sun Pharmaceutical Industries, Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 28, 2016
Calcium Gluconate 1% -- 1000 mL VIAFLEX IV BAG, Rx only, THE APOTHECARY, A COMPOUNDING PHARMACY, 165 19th St S #102,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W & C dba The Apothecary
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 28, 2016
Amoxicillin For Oral Suspension, USP - Dye Free, 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.West-Ward Pharmaceuticals Corp.
FDA (openFDA drug enforcement)
Reported Sep 21, 2016
buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amerisource Health Services
FDA (openFDA drug enforcement)
Reported Sep 21, 2016
Pantoprazole Sodium Delayed-Release Tablets USP, 40 mg Rx Only, 90 tablets per bottle, Manufactured for Aurobindo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aurobindo Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Sep 21, 2016
DOBUTamine Injection, USP 250 mg/20 mL, 20 mL Vial, For IV Use Only, Must be Diluted Prior to Use, (12.5 mg per mL), Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
FDA (openFDA drug enforcement)
Reported Sep 14, 2016
Ephedrine Sulfate Injection, USP, 50 mg/mL, Single Dose Vial, packaged in a) 1 mL fill in a 2 mL Vial (NDC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allergy Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported Sep 14, 2016
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerisource Health Services
9 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 14, 2016
Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection, 10 mL multidose vial, sterile. Rx only. Compounded by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Isomeric Pharmacy Solution, LLC
FDA (openFDA drug enforcement)
Reported Sep 14, 2016
Amlodipine Besylate Tablets USP, 2.5mg, 90-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Limited
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 14, 2016
Selegiline HCL Tablets USP 5mg, 60- count bottles, Rx only, Manufactured by: Stason Pharmaceuticals, Inc. Irvine, CA…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stason Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Sep 14, 2016
ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL) , Rx Only, Manufactured in Hungary for TEVA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva North America
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 14, 2016
Bromocriptine Mesylate Capsules USP, 5 mg, 30-count bottles, Rx only, Manufactured by: Cadila Healthcare ltd.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals USA 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.