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 20, 2012
Carbon Dioxide, USP, Medical Gas, packaged in a) size EA aluminum, CGA940 (CDUSPEA), b) size E CGA 940 (CDUSPE), c) 50…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Airgas Inc.
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
Murocel (methylcellulose) Lubricant Opthalmic Solution (USP, 1%), 15 mL bottle, OTC, Manufactured by Bausch & Lomb…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb, Inc.
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
Midazolam HCl Injection, 5 mg/mL, 1 mL single use vials, packaged in 10 x 1 mL single use vials per pack, Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ben Venue Laboratories Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only, Manufactured…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Endo Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
Propofol Injectable Emulsion, 1%, (10mg/mL), packaged in a) 200 mg/20 mL, 5 Units x 20 mL Single patient infusion vials…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira, Inc.
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4% a) 30 mL SINGLE DOSE VIAL, (NDC 0517-2930-25), b) 100 mL PHARMACY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luitpold Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15-count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Medical Technologies a Pfizer Company
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
Daytrana (methylphenidate) transdermal system patch, Delivers 20 mg over 9 hours (2.2 mg/hr), 1 patch per pouch,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noven Pharmaceuticals, Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
Arthrotec 75 (diclofenac sodium and misoprostol) tablets, 75 mg/200 mcg, a) 30-count tablets per bottle (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physicians Total Care, Inc.
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
DermaZinc Spray, 0.25% zinc pyritione, topical OTC, 4 fl oz bottle Distributed By: Dermallogix Partners, Inc.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Quadrant Chemical Corporation
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.