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 May 13, 2015
C-Topical 4% CII (cocaine hydrochloride), topical solution, 4 ml bottle, (NDC 0527-1728-74), Rx Only, Manufactured for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cody Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported May 13, 2015
EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Detox Transforms
4 more products in this recall
FDA (openFDA drug enforcement)
Reported May 13, 2015
0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
FDA (openFDA drug enforcement)
Reported May 13, 2015
Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resale or Dispensing to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physician Preferred Medical, LLC
FDA (openFDA drug enforcement)
Reported May 13, 2015
Forever Beautiful INFINITY, capsules, 300mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
High riskUsing this product could cause serious injury, illness or death — stop using it now.REFA Enterprises, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 13, 2015
KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
FDA (openFDA drug enforcement)
Reported May 13, 2015
Alinia (nitazoxanide), powder for oral suspension, 100mg/5mL, 60 mL/bottle. Rx only, Manufactured for Lupin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Romark Laboratories, L.C.
FDA (openFDA drug enforcement)
Reported May 13, 2015
ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70, Extracto de semilla de Sen 47.6, Lagrima de Coix 42,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ultra ZX Supplements
FDA (openFDA drug enforcement)
Reported May 13, 2015
Captopril Tablets, USP 12.5 mg, Rx Only, a) 100 count bottles NDC 64679-902-01, b) 1000 count bottles NDC 64679-902-02,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wockhardt USA Inc.
FDA (openFDA drug enforcement)
Reported May 6, 2015
Ketorolac Tromethamine Inj. USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 6, 2015
Fluoxetine Capsules USP, 10 mg, in 100-count bottles, Rx only, Manufactured by Pliva Krakow Pharmaceutical Company…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Apr 29, 2015
5-Aminolevulinic Acid Hydrochloride active pharmaceutical ingredient packaged in varying grams or kg in bags or drums,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Attix Pharmaceuticals
469 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 29, 2015
Fluorescein Sodium Ophthalmic Strips USP, 0.6 mg per strip, labeled as 1) Fluorescein GloStrips, individually wrapped…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nomax Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 29, 2015
Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Reckitt Benckiser LLC
FDA (openFDA drug enforcement)
Reported Apr 29, 2015
Droperidol injection, 2.5 mg/mL, 5 mg Total Dose, 2 mL Fill Volume per syringe, packaged in 10-count syringes per heat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SCA Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Apr 29, 2015
Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tarmac Products, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 22, 2015
Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis Laboratories, FL, Inc.
FDA (openFDA drug enforcement)
Reported Apr 22, 2015
Flurandrenolide Tape, USP, 4 mcg per sq cm, Rx Only. Distributed By: Actavis Pharma, Inc., Parsippany, NJ 07054,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis Laboratories
FDA (openFDA drug enforcement)
Reported Apr 22, 2015
Bromfenac Ophthalmic Solution 0.09%, Rx Only. Mfg For: Apotex Corp., Weston, FL, 33326. Available in a) 1.7 mL Bottle,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Apotex Inc.
FDA (openFDA drug enforcement)
Reported Apr 22, 2015
Potassium Chloride, microencapsulated extended-release tablets, 20 mEq, blister card of 30/10 cards in a corrugated…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cardinal Health
FDA (openFDA drug enforcement)
Reported Apr 22, 2015
Minivelle (estradiol transdermal system) 0.05 mg/day, 8-count box, Rx only, Manufactured by Noven Pharmaceuticals,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noven Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Apr 15, 2015
0.9% Sodium Chloride Injection USP, 100 mL MINI-BAG Plus Container, Rx only, Baxter Healthcare Corporation, Deerfield,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corp.
FDA (openFDA drug enforcement)
Reported Apr 15, 2015
University of Alabama Birmingham TPN Neonatal Starter Bag, compound vol: 100 ml, Trophamine 4% Dextrose 10%, sterile…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Central Admixture Pharmacy Services, Inc.
33 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 15, 2015
GLIPIZIDE and METFORMIN HYDROCHLORIDE Tablets, USP, 2.5 mg/500 mg, 100 ct Bottles, Rx Only. Manufactured for: Heritage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Pharmaceuticals, 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.