All recall categories

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.

Drugs

Reported Sep 13, 2017

Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Mckesson Packaging Services

FDA (openFDA drug enforcement)

Drugs

Reported Sep 6, 2017

Ketorolac Tromethamine Injection, USP 30 mg/mL, packaged in 1 mL single-dose vials, Rx only, Amphastar Pharmaceuticals,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amphastar Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Sep 6, 2017

Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Morton Grove Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Sep 6, 2017

Morphine Sulfate Oral Solution, 100 mg/ 5 mL (20 mg/mL), packaged in a 1 oz. bottle containing 30 mL with an oral…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tris Pharma Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Aug 30, 2017

CaverFlo Natural Herbal Coffee, 25 g, supplied in boxes of 10 packets, manufacture for Caverflo Texas Trading -- UPC:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Brian P. Richardson

FDA (openFDA drug enforcement)

Drugs

Reported Aug 30, 2017

Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

C. O. Truxton

5 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Aug 30, 2017

Phentermine Capsules, 15 mg, a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) 21-count…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

PD-Rx Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Aug 30, 2017

Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Harvard Drug Group

4 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL Unit Dose Cup, a) unit dose cup (NDC 50383-720-15), b) 100-count tray…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Akorn Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manufactured…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amgen, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Voriconazole Tablets, 200 mg, 20-count cartons (4 x 5) Unit Dose, Rx only, Manufactured for: AvKARE, Inc. Pulaski, TN…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

AVKARE Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Dynamic Technical Formulations

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Genetic Edge Compounds LLC

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz)., 1250 servings, Packed By:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Global Marketing Enterprises, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hardcore Formulations

1 more product in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Entecavir Tablets 0.5 mg, 30 tablets per container, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc.,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hetero USA Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

KVK-Tech, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Beautipharm All Day Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl methoxycinnamide 4%) Facial Cream, 1.66 oz. Net.…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Linde Eckstein GmbH + Co. KG

13 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Aug 23, 2017

Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02 mg chewable and ferrous Fumarate 75 mg) Tablets,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lupin Limited (Unit 1)

FDA (openFDA drug enforcement)

Drugs

Reported Aug 16, 2017

Oxygen Refrigerated Liquid USP UN 1073, Rx only, At Home Medical 200 American Road, Morris Plains, NJ…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

AtHome Medical, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Aug 16, 2017

Ephedrine Sulfate in 0.9% Sodium Chloride 10 mL, 50 mg/10 mL (5 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cantrell Drug Company

17 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Aug 16, 2017

Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial. Mfd For: Teva Parenteral…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hospira Inc., Lake Forest

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Aug 16, 2017

Glipizide Extended-Release Tablets (anti-diabetic agent), 5 mg, packaged in 30-unit dose blister pack per carton, Rx…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Teva Pharmaceuticals USA

FDA (openFDA drug enforcement)

Drugs

Reported Aug 16, 2017

Nystatin Topical Powder, USP, 100,000 USP units per gram, 15 grams per bottle, Rx only, Vensun, NDC 42543-052-61

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

X-Gen 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.