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Browse Drug Recalls

3 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 3 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 3 FDA drug recalls.

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DateProductReasonClassFirm
Dec 23, 2015 La' Trim Plus Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufac... Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolp... Class I Bee Xtreme
Dec 23, 2015 Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured f... Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolp... Class I Bee Xtreme
Dec 23, 2015 Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles, Manufactured for... Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolp... Class I Bee Xtreme

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.