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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 27, 2015 MIRACLE ROCK 48 capsules, packaged in 2 x 2-count blisters, 4-count capsules ... Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain undeclared thiosilden... Class I The One Minute Miracle Inc
Aug 27, 2015 MIRACLE DIET 30 capsules, 30-count bottle, Manufactured Exclusively For: The ... Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain undeclared phenolphth... Class I The One Minute Miracle 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.