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.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Dec 10, 2013 | Dream Body Slimming Capsule (Chinese bitter orange 24%, Cassia Seed 18%, Aloe... | Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and . Sibutram... | Class I | Slim Beauty USA |
| Dec 10, 2013 | Dr. Ming's Chinese Capsule (Ginger 50 mg, Camellia Sinensis 50 mg, Malus Dome... | Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and phenolphth... | Class I | Slim Beauty USA |
| Dec 10, 2013 | Magic Slim capsules (Ling Zhi, Ebony, Fox-nut, Tuckahoe, Seman Pruni, Dioscor... | Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and phenolphth... | Class I | Slim Beauty USA |
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.