Recall archive / FDA drug enforcement
Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, ... — FDA record D-0382-2025
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Apr 15, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-403-02
- Reason
- cGMP deviations
- Classification
- Class II
- Recalling firm
- Pharmadel, LLC
- Quantity
- 6,048 bottles
- Agency-reported status
- Terminated
- Source record identifier
- D-0382-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lot, expiry: EAG-01, EXP: MAR 27 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
DE
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Apr 30, 2025
- Recall initiation date
- Apr 15, 2025
- Center classification date
- Apr 21, 2025
- Termination date
- Jan 8, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.