Browse Drug Recalls

2,157 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 2,157 FDA drug recall enforcement actions. Each entry includes the product description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Drug Safety Recalls

Browse 2,157 FDA drug recalls.

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DateProductReasonClassFirm
Jun 14, 2012 Kleenex Foam Hand Sanitizer, Alcohol Free in a) 1.5 fl oz. (45mL) , b) 8 fl o... Microbial Contamination of Non-Sterile Products; The affected lots were found to be contaminated ... Class II Kimberly-Clark Corporation
Jun 14, 2012 Dukal Corporation BZK Swab, First Aid Antiseptic, (Benzalkonium Chloride), 0.... Microbial contamination of Non Sterile Product; contamination with Burkholderia cepacia (manufact... Class II Dukal Corp.
Jun 7, 2012 Erythromycin Topical Solution USP, 2%, 60 mL bottle with applicator, Rx only.... Chemical Contamination: This product is being recalled because trace amounts of a plasticizer (Di... Class III Fougera Pharmaceuticals, Inc.
May 8, 2012 Estradiol Hemihydrate M20 EP/USP Powder, packaged in a) 1.5 kg and b) 2.5 kg ... Cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due... Class II Bayer HealthCare Pharmaceuticals Inc.
Feb 8, 2012 Lipitor (Atorvastatin calcium); 40 mg, 30 TABLETS, Rx only, Repacked & distri... Chemical Contamination: Complaints of an uncharacteristic odor identified as 2,4,6 tribromoanisole. Class II Physicians Total Care, Inc.
Feb 10, 2011 Earth Force, Ltd., Power Towels, QS Plus Hand Sanitizing Wipes (antiseptic), ... Chemical Contamination: QS Plus wipes were found to be contaminated with different substance (782... Class III Abc Compounding Company Inc
Feb 8, 2011 Plavix 75 mg, 30 count bottle, NDC (54868-4070-0), Rx only, Manufactured by B... Chemical Contamination: Uncharacteristic moldy odor due to presence of 2,4,6-tribromoanisole (TBA). Class III Physicians Total Care, Inc.

Frequently Asked Questions

When a drug safety issue is identified, through FDA inspections, laboratory testing, adverse event reports, or manufacturer quality checks, the responsible company issues a recall to remove the affected products from the market. Pharmacies pull the product from shelves, and consumers are advised to contact their healthcare provider for alternatives.

The leading causes include cGMP deviations, impurity contamination (including nitrosamines like NDMA), failed dissolution or stability testing, sterility issues, potency problems, labeling errors, and foreign particle contamination.

Use the search and filter tools on this page to look up specific medications, active ingredients, or manufacturers. Each recall entry includes the product description, lot numbers, and distribution details.