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 Jun 26, 2019
Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented), a) 15 gram (NDC 52565-019-15) and b) 50 gram (NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teligent Pharma, Inc.
FDA (openFDA drug enforcement)
Reported Jun 26, 2019
ANASTROZOLE Tablets, 1 mg, Rx Only, 30-count bottle, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals USA Inc.
13 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Heparin Sodium 25,000 USP units per 250 mL (100 USP units per mL) in 5% Dextrose Injection, 250 mL EXCEL Container bag,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical Inc.
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Lotemax (loteprednol etabonate ophthalmic gel 0.5%), Sterile, Rx Only, 5 g box, Bausch & Lomb, a division of Valeant…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bausch & Lomb
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Sevoflurane, USP Inhalation Anesthetic 250 mL bottles, Rx only, Manufactured for Baxter Healthcare Corporation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
ZYFLO CR (zileuton) extended-release tablets, 600 mg, 120-count bottles, Rx only, Distributed by Chiesi USA, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chiesi USA, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Ondansetron Injection, USP, 40 mg / 20 mL, 20 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
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Senna (sennosides 8.8 mg) Syrup, 8 fl oz. (237 mL) bottles, Rij Pharmaceuticals Corporation 40 Commercial Avenue,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Geritrex, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Estradiol Vaginal Inserts USP 10 mcg, packaged in box of 8 Vaginal Inserts (with disposable applicators), Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Glenmark Pharmaceuticals Inc., USA
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
PROCHLORPERAZINE EDISYLATE INJECTION, USP 10 mg/2mL (5mg/mL), 2mL Vial, Rx Only, Mfg by: Emcure Pharmaceuticals Ltd.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heritage Pharmaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Pecgen DMX Cough Suppressant Expectorant, Contains the same active ingredients as Trispec DMX, Sugar Free, Alcohol…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Novis PR, Inc.
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Bacteriostatic Water for Injection, 10 mL vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharm D Solutions, LLC
17 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Select Distributions LLC
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthetopes Inc.
7 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
RisperiDONE Oral Solution, USP, 1 mg/mL, Rx Only, 30 mL bottle, NDC 13668-589-06, Manufactured by Bio-Pharm Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
40 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 5, 2019
Bevacizumab 2.5 mg/0.1 mL, packaged in a Prefilled Syringe, Rx only, AVELLA SPECIALTY PHARMACY 24416 N. 19TH AVENUE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avella of Deer Valley, Inc. Store 38
FDA (openFDA drug enforcement)
Reported Jun 5, 2019
ANTIBACTERIAL Foaming Hand Wash With Moisturizers labeled as Antibacterial Foaming Soap, ACTIVE:P.C.M.X, packaged in a)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inopak Ltd.
9 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 5, 2019
Cefdinir for Oral Suspension USP, 250mg/5mL, Powder for oral suspension, 60 mL bottle, Rx only, Manufactured for: Lupin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jun 5, 2019
The Beast, The Beast can be taken under the situation of Heart disease and even after drinking, 4600 mg X 4 Capsules…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stiff Boy LLC
FDA (openFDA drug enforcement)
Reported May 29, 2019
Losartan Potassium Tablets USP 25 mg 30 count bottle NDC 60429-316-30 Rx only GSMS Incorporated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Medical Supply Inc.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported May 29, 2019
Losartan Potassium Tablets, USP 50 mg 1000 film coated tablets Rx Only Manufactured by: Vivimed Life Sciences Private…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Pharmaceuticals, Inc.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported May 29, 2019
Amitiza (lubiprostone) capsules, 8 mcg, 60-count bottle, Rx only, Manufactured by: Sucampo Pharma Americas, LLC, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mallinckrodt Pharmaceuticals
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 29, 2019
Promacta (eltrombopag) 12.5 mg for Oral Suspension, Rx Only Manufactured by: Halo Pharmaceuticals, Inc. Whippany, New…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Novartis Pharmaceuticals Corp.
FDA (openFDA drug enforcement)
Reported May 29, 2019
Articaine DENTAL, Articane hydrochloride 4% and epinephrine 1:100,000, 50 cartridges. 1.7 mL each, Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Septodont 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.