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 16, 2019
Optiray 320 (ioversol) Injection 68%, 320 mg/mL Organically Bound Iodine, packaged in 1 - 100 mL Ultraject Prefilled…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Guerbet LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 16, 2019
Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Morton Grove Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Oct 16, 2019
Rifampin for Injection, USP, 600 mg/vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103; NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mylan Laboratories Limited (Sterile Products Division)
FDA (openFDA drug enforcement)
Reported Oct 16, 2019
10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Oct 16, 2019
Sandoz Ranitidine Hydrochloride Capsules 150mg 60 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ Product of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 16, 2019
Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30 count bottle, Rx only, Manufactured by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Oct 16, 2019
DrKids Children's Natural Cough Syrup English Ivy Leaf, packaged in Pre-measured Single-Use Vials 0.17 fl. oz. (5 mL)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unipharma, Llc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 9, 2019
Phenylephrine Hydrochloride Ophthalmic Solution, USP, 2.5%, 15 mL bottle, Rx only, Mfd. by: Akorn, Inc., Lake Forest,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn, Inc.
FDA (openFDA drug enforcement)
Reported Oct 9, 2019
Vivitrol (naltrexone for extended-release injectable suspension) 380 mg/vial. Each Carton Contains: 1) One vial of 380…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alkermes, Inc.
FDA (openFDA drug enforcement)
Reported Oct 9, 2019
C-ACETYLCYSTEINE OPHTH 10% SOLN, packaged in a) 5 mL and b) 10 mL droptainer bottles, Rx only, Colonia Care Pharmacy,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Colonia Care Pharmacy
31 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 9, 2019
Alpha Lipoic Acid (PF) 750 mg/30 mL (25 mg/mL) 30 mL Single Dose Vial for IV Use, Rx Only, KRS Global Biotechnology 791…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KRS Global Biotechnology, Inc.
79 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 9, 2019
Losartan Potassium Tablets, USP 50mg, 1000 tablets per bottle, Rx Only, Manufactured for: Torrent Pharma Inc., Basking…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
Lidocaine Hydroclhoride Jelly USP, 2%, 30 mL tubes, Rx Only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn, Inc.
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
Nucala (mepolizumab) Injection, 100 mg/mL Prefilled Syringe, Single-Dose, For subcutaneous use only, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health dba Specialty Pharmaceutical Services
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
Quinacrine Dihydrochloride (98.25%), bulk API product, packaged in a) 500 g NDC# 71052-530-05; b) 50 g NDC#…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Darmerica, LLC
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
minolira (minocycline hydrochloride) extended-release tablets 135 mg* Physician Sample Not for Sale 5 Tablets, Rx Only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.EPI Health, LLC
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
Fentanyl Citrate Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson Matthey Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
ethosuximide capsules, USP, 250 mg, 100-count bottle, Rx Only, Distributed by: Greenstone LLC Peapack, NJ 07977 Made in…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
Fexofenadine HCl Tablets, 180 mg, Pkg Size 90, Mfg: Aurohealth LLC, Repackaged by Preferred Pharmaceuticals, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
Natpara (parathyroid hormone) for Injection, 25 mcg/dose, 2 pack cartridges, Rx only, For subcutaneous use only,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shire Human Genetic Therapies, Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 25, 2019
Fexofenadine Hydrochrloride Tablets USP, 180 mg, 100-count bottle, Distributed by: Aurohealth LLC., 2572 Brunswick…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aurolife Pharma, LLC
10 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 25, 2019
PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream, 4%, packaged in a) 1 OZ (NDC 69804-002-05), b) 2 OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ridge Properties, LLC
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 25, 2019
Anagrelide Capsules, USP, 0.5 mg, 100-count bottle, Rx only, Manufactured in India for: Torrent Pharma Inc., Basking…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
FDA (openFDA drug enforcement)
Reported Sep 25, 2019
Oxcarbazepine Oral Suspension, USP, 300 mg/5 mL, 250 mL per bottle, Rx Only, Distr. by: West-Ward…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.West-Ward Columbus 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.