Rapidol Arnica recalls
The FDA has published 2 recalls involving Rapidol Arnica since 2025. The latest was reported on 30 Apr 2025. Most were for manufacturing (cgmp) deviations. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls2since 2025
Last 12 months0reported
Class I00% of total
Ongoing0latest 30 Apr 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why rapidol arnica is recalled
Companies
By year
All rapidol arnica recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Rapidol Arnica Tablets, Homeopathic Medicine recalled by Pharmadel | Pharmadel | Manufacturing (CGMP) Deviations | DE |
| Drug | CLASS II | Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine recalled | Pharmadel | Manufacturing (CGMP) Deviations | DE |
Should you stop taking Rapidol Arnica?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.