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Browse Drug Recalls

2 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 2 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 FDA drug recalls.

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DateProductReasonClassFirm
Jul 26, 2012 Ventolin HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200... Does Not Deliver Proper Metered Dose: Potential content of albuterol per dose is below specificat... Class II GlaxoSmithKline Inc
Jun 4, 2012 Trizivir (abacavir sulfate 300mg, lamivudine 150 mg and zidovudine 300 mg), 6... Adulterated Presence of Foreign Tablets: Trizivir 300/150/300 mg tables, Lot 0ZP5128 may incorrec... Class II GlaxoSmithKline 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.