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Browse Drug Recalls

4 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 4 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 4 FDA drug recalls.

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DateProductReasonClassFirm
Jul 18, 2019 Neomycin Sulfate 3.5 mg/Polymyxin B Sulfate 10,000 units/Dexamethasone 1 mg ... CGMPs Deviations: Insufficient Quality Assurance controls over critical systems in the manufactur... Class II Preferred Pharmaceuticals, Inc
Feb 26, 2018 Evamist (estradiol transdermal spray), 1.53mg estradiol/spray, 0.27 fl oz (8.... Defective Delivery System: Potential that cracks in the vial neck near the crimp may result in pr... Class II Paddock Laboratories, LLC.
Mar 11, 2014 Perrigo, Clindamycin Palmitate Hydrochloride for Oral Solution, USP, 75mg/5m... Presence of Particulate Matter Perrigo is recalling seven lots of Clindamycin Palmitate Hydrochlo... Class II Paddock Laboratories, LLC
Oct 3, 2012 Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., M... Paddock Laboratories, LLC are recalling one lot (2012028142) of Moexipril HCl Tablets 7.5mg (ex... Class II Paddock Laboratories, LLC

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.