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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
Aug 23, 2012 Mojo Nights for Her, 1 capsule, UPC 7 18122 12133 5, Distributed By: Mojo Hea... Marketed Without an Approved NDA/ANDA: The products were found to contain FDA approved ingredien... Class I Evol Nutrition
Aug 23, 2012 Mojo Nights, 1 capsule, UPC 7 18122 11983 7, Distributed By: Mojo Health Laud... Marketed Without an Approved NDA/ANDA: The products were found to contain FDA approved ingredien... Class I Evol Nutrition

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.