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Browse Drug Recalls

10 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 10 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 10 FDA drug recalls.

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DateProductReasonClassFirm
Jan 24, 2014 Slim Xtreme Weight loss capsules, 500 mg, supplied in 30 count bottles, Anoth... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, Inc.
Jan 24, 2014 Magic Slim capsules, supplied in 60 count bottles, distributed by MyNicKnaxs,... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, Inc.
Jan 24, 2014 REDUCE WEIGHT FRUTA PLANTA Capsules, 400 mg, supplied in 30 count boxes, dist... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, Inc.
Jan 24, 2014 Super Fat Burning Bomb Capsules, 400 mg, supplied in 30 count boxes, distribu... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, Inc.
Jan 24, 2014 JIANFEIJINDAN Activity Girl Capsules, 400 mg, supplied in 30 count boxes, dis... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared ingredient: N-di-d... Class I MyNicNaxs, Inc.
Jan 24, 2014 SlimEasy Herbs Capsule, 400 mg, supplied in 30 count boxes, distributed by My... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, Inc.
Jan 24, 2014 Pill for weight reduction, (Japanese Chinese Formula from Japan Hokkaido Cang... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, Inc.
Jan 24, 2014 Meizi Evolution Soft Gel Capsules, supplied in 30 count bottles, distributed ... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, Inc.
Jan 24, 2014 Meizitang Strong Version Botanical Slimming, Soft Gel Capsules, 650 mg, suppl... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, Inc.
Jan 24, 2014 Fruta BIO 400 mg capsules, supplied in 30 count boxes, distributed by MyNicKn... Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceuti... Class I MyNicNaxs, 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.