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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
Mar 29, 2021 69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and ... Class I Nuri Trading LLC
Mar 29, 2021 Thumbs Up 7 Black 25K capsule, packaged in a) 1-count blister card and b) 10-... Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil, an ... Class I Nuri Trading LLC
Mar 29, 2021 Thumbs Up 7 White 11K capsule, packaged in a) 1-count blister card and b) 10-... Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil sild... Class I Nuri Trading LLC
Mar 29, 2021 Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count bo... Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and ... Class I Nuri Trading 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.