Browse Drug Recalls

6 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 6 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 6 FDA drug recalls.

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DateProductReasonClassFirm
Feb 7, 2025 Voriconazole Container Description: voriconazole The product packed in white ... CGMP Deviations Class II Aspen Biopharma Labs Pvt., Ltd.
Feb 7, 2025 Latanoprost NDC# 82187-1002-1 Container Description: Amber colour bottle CGMP Deviations Class II Aspen Biopharma Labs Pvt., Ltd.
Feb 7, 2025 Bimatoprost NDC# 82187-1001-1 Container description: The product packed in ... CGMP Deviations Class II Aspen Biopharma Labs Pvt., Ltd.
Feb 7, 2025 Alprostadil Container Description: Amber color bottle CGMP Deviations Class II Aspen Biopharma Labs Pvt., Ltd.
Feb 7, 2025 Finasteride NDC# 82187-1003-1 Container Description: The product packed in w... CGMP Deviations Class II Aspen Biopharma Labs Pvt., Ltd.
Feb 7, 2025 Chlorambucil Container Description: The product packed in double self-seal co... CGMP Deviations Class II Aspen Biopharma Labs Pvt., Ltd.

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.