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 Aug 9, 2017
Amantadine HCl Capsules, USP, 100 mg, Rx Only, 50 Capsules (5x10) Unit Dose Cartons, Manufactured for: AvKARE Inc,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apace KY LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Alka-Seltzer Original ( 325 mg Aspirin (NSAID), 1916 mg Analgesic, Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer HealthCare Pharmaceuticals, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Pravastatin Sodium Tablets, USP, 10 mg, packaged in a) 90-count bottles (NDC 55111-229-90) and b) 500-count bottles…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dr. Reddy's Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Potassium Phosphates Inj., USP, 45 mM (3 mM P/mL) Also contains: 66 mEq K+ (4.4 mEq/mL) 15 mL, Single-dose, Caution:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira a Pfizer Company
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PD-Rx Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Carbamazepine Oral Suspension, USP. 100 mg/5 mL, 5 mL Unit Dose Cups, Rx Only, Pkg: Precision Dose, Inc., S. Beloit, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Precision Dose Inc.
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Albuterol Sulfate Inhalation Solution, 0.021% (0.63 mg/3mL), packaged in 5 pouches of 5 x 3mL Sterile Unit-Dose Vials…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Ibuprofen Tablets, USP 600 mg, 500-count bottle (Capsule Shaped), Rx only, Manufactured for: Time Cap Labs, Inc., 7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Time-Cap Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Magnesium Citrate Oral Solution, packaged in a 10 fl. oz. (296 mL) glass bottle, OTC, labeled as: a) GoodSense…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vi-Jon, Inc.
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Lactulose Solution, USP, 10 g/15 mL, dose cups delivers 15 mL packaged in 50-unit dose cups per case, Manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Divalproex Sodium Delayed Release Tablets, USP, 125 mg, 100-count bottle Rx only, Manufactured by Cadila Healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals USA Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 2, 2017
morphine sulfate 1 mg per mL in 0.9% Sodium Chloride, (Total morphine Dose 100 mg/100 mL), Total Volume 100 mL Single…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SCA Pharmaceuticals
35 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 26, 2017
Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Gland Pharma…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hospira Inc., A Pfizer Company
FDA (openFDA drug enforcement)
Reported Jul 26, 2017
Succinylcholine Chloride Injection (Preserved) 20 mg per mL, 200 mg per 10 mL, 10 mL Total Volume in BD Syringe, For IV…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PharMedium Services, LLC
12 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 26, 2017
Mefenamic Acid, 250mg capsules, packaged in 30-count bottles, Rx Only, Distributed by: Prasco Laboratories Mason, OH…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Shionogi Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 26, 2017
Buprenorphine and Naloxone Sublingual Tablets, 2 mg/0.5 mg 30 tablets per bottle, Rx only, Distributed by: Teva…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 26, 2017
Obagi-C Rx System C-Therapy Night Cream, Net wt. 2 oz. (57g) bottle, Rx only, Distributed by OMP, Inc., Long Beach, CA…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Valeant Pharmaceuticals North America LLC
FDA (openFDA drug enforcement)
Reported Jul 19, 2017
QUELICIN (Succinylcholine Chloride) Injection, USP 20 mg/mL in a) 5 mL vial (NDC 15082-814-67), b) 7mL vial (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Pharma Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 19, 2017
BRILINTA (ticagrelor) tablets, 90 mg, 8-count Professional Sample bottles, Rx only, Mfd. for: AstraZeneca…
High riskUsing this product could cause serious injury, illness or death — stop using it now.AstraZeneca Pharmaceuticals, LP
FDA (openFDA drug enforcement)
Reported Jul 19, 2017
0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 19, 2017
EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bristol-myers Squibb Company
FDA (openFDA drug enforcement)
Reported Jul 19, 2017
Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jul 19, 2017
UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules, supplied in 2, 4 and 10 count packages,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Organic Herbal Supply
10 more products in this recall
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.