D-0382-2025 Class II Terminated
FDA drug recall D-0382-2025 was initiated by Pharmadel, LLC on April 15, 2025 and is designated Class II. Reason for recall: cGMP deviations The recall status is terminated (terminated January 8, 2026). Affected quantity: 6,048 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- April 30, 2025
- Initiation Date
- April 15, 2025
- Termination Date
- January 8, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 6,048 bottles
Product Description
Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-403-02
Reason for Recall
cGMP deviations
Distribution Pattern
DE
Code Information
Lot, expiry: EAG-01, EXP: MAR 27