Browse Drug Recalls
6 FDA drug safety recalls.
FDA Drug Recall Enforcement Database
Browse 6 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 6 FDA drug recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Apr 15, 2025 | Rapidol Arnica Tablets, Homeopathic Medicine, 100-count bottle, Distributed b... | cGMP deviations | Class II | Pharmadel, LLC |
| Apr 15, 2025 | DoloEar Earache Drops, Homeopathic, 0.50 oz fl (15 mL), Distributed by: Pharm... | cGMP deviations | Class II | Pharmadel, LLC |
| Apr 15, 2025 | Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distribut... | cGMP deviations | Class II | Pharmadel, LLC |
| Apr 15, 2025 | Kingskin, Elimina Las Verrugas, For the removal of common warts, 0.50 oz fl (... | cGMP deviations | Class II | Pharmadel, LLC |
| Apr 15, 2025 | DoloDent Maximum Strength Toothache Drops, Homeopathic Oral Drops, 0.50 oz fl... | cGMP deviations | Class II | Pharmadel, LLC |
| Apr 15, 2025 | Urodel, Urinary Tract Infection Symptoms Relief, Homeopathic, 30 chewable tab... | cGMP deviations | Class II | Pharmadel, LLC |
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.