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 Aug 13, 2014
Risperdal CONSTA (risperiDONE), 25 mg Dose Pack, Rx Only, Single Use Only Janssen Pharmaceuticals Inc., Titusville, NJ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Janssen Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Aug 13, 2014
Alprazolam Tablets, USP 0.25 mg, UD 100 Tablets (10 x 10), Rx Only, Mfg By: Sandoz, Inc., Princeton, NJ 08540 --- NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Packaging Services
FDA (openFDA drug enforcement)
Reported Aug 13, 2014
Vitamin B12 Methylcobalamin with MIC Injection USP 1000 mcg/ml, Sterile, 10 ml vial and 30 ml vial. For IM or Deep SQ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Supply Liquidators LLC
14 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 13, 2014
Cataflam (diclofenac potassium) tablets, 50 mg, 100-count bottles, Rx only, Manufactured by: Patheon Inc., Whitby…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Pharmaceuticals Corp.
FDA (openFDA drug enforcement)
Reported Aug 13, 2014
Tetrahydrozoline HCL, 16 kg drum. Societa Italiana Medicinali Scandicci (S.I.M.S.), Made in Italy. NDC 12660-0048 CAS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SST Corporation
FDA (openFDA drug enforcement)
Reported Aug 13, 2014
buPROPion HCl Extended-Release Tablets, USP (SR), 100 mg, 500-count bottle, Rx Only, Manufactured by: Wockhardt…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wockhardt USA Inc.
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
OXYCODONE HYDROCHLORIDE C II Oral Solution USP, 5 mg/5 mL, 15 mL Vial, Rx only. Boehringer Ingelheim, Roxane…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Boehringer Ingelheim Roxane Inc.
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
Azor Tablets (amlodipine and olmesartan medoxomil) 10 mg*/40 mg, 30 count bottles, Rx Only, Manufactured for: Daiichi…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daiichi Sankyo Pharma Development
7 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
Dermamedics Post Procedure Cream, 1 ounce containers which were distributed with a SKU number of DM 1026
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dermamedics, LLC
8 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
Fagron, Phytobase Cream, 500 g, Article number: 802156. RX only, For prescription compounding Natural self-emulsifying…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fagron, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jubilant Cadista Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
Aspirin DR Enteric Coated Tablets, USP 325 mg, UD 750 tablets (25x30), Dist. By: McKesson Packaging Services a business…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mckesson Packaging Services
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
Cardura XL (doxazosin mesylate extended release tablets, 4 mg, 30-count bottle, Rx only, Distributed by Roerig Division…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
Alprazolam Tablets, USP, 0.25mg, Rx only, 1000 tablets, Sandoz Inc., Princeton, NJ --- NDC 0781-1061-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz Incorporated
FDA (openFDA drug enforcement)
Reported Aug 6, 2014
triple therapy, LANSOPRAZOLE DR Capsules USP 30mg, CLARITHROMYCIN Tablets USP 500mg, AMOXICILLIN Capsules USP 500mg, 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Jul 30, 2014
DENBLAN Anticavity Fluoride Toothpaste, Whitening formula, sodium monofluorophosphate 0.76%, 2.6 oz/75 mL tube,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Estee Lauder Inc.
FDA (openFDA drug enforcement)
Reported Jul 30, 2014
Levofloxacin 750 mg/250 mL D5W, Trinity Care Solutions, 202-C SW 17th Street, Ocala, FL 34471-5138, For Parenteral Use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Franck's Lab Inc. dba Trinity Care Solutions
29 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 30, 2014
Orphenadrine Citrate Extended Release Tablets, 100 mg a)100-count bottle, (NDC 0185-0022-01) b) 1000-count bottle, (NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sandoz Inc.
FDA (openFDA drug enforcement)
Reported Jul 30, 2014
Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged and labeled as Thiamine. Re-Packaged By: Shamrock Medical…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shamrock Medical Solutions Group LLC
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 30, 2014
Clonidine HCl Injection, 1000 mcg/10 mL (100 mcg/mL),10 mL Single Dose Vial, Rx only, Manufactured for: X-Gen…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.X-Gen Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jul 23, 2014
ChloraPrep With Tint, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), 26 mL APPLICATOR,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 213, LLC
FDA (openFDA drug enforcement)
Reported Jul 23, 2014
Triamcinolone Acetonide Lotion USP, 0.1%, 60 mL Bottle, Rx Only, For Dermatologic Use Only, Not for Ophthalmic Use, E.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Fougera Pharmaceuticals Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 23, 2014
Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, C-II, (50 mcg/mL), 50 mL Single-dose Fliptop Vial, Rx only.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
FDA (openFDA drug enforcement)
Reported Jul 23, 2014
Diltiazem HCl Extended-release Capsules, USP, 120 mg, packaged in 80 Capsules (8 x 10) blister cards per carton, Rx…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
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.