Menthol Recall: Dr. Bump Natural Pain Relief Gel
Announced 2025-12-03 · FDA
The FDA is recalling 4,890 bottles of Dr. Bump Natural Pain Relief Gel, Menthol 5%, Lot D54947, exp 4/30/2028, due to CGMP deviations. The product was distributed in CA, CO, FL, PR, and WA. Corrective action details were not provided.
| Brand | CA BOTANA International, Inc. |
|---|---|
| Product | Dr. Bump Natural Pain Relief Gel, Menthol 5%, NET WT 4 FL OZ/118 ML per bottle, Distr. by 1Beauty US LLC, Palm Desert, CA 92211. NDC: 35192-052-18, UPC 8 18204 02513 8 |
| Reason | CGMP Deviations |
| Severity | moderate |
| Units affected | 1492 |
| Distribution | CA, CO, FL, PR, WA |
| Agency | FDA |
| Recall / campaign no. | Lot D54947, exp 4/30/2028 |
WHAT YOU SHOULD DO
- Stop using any recalled Dr. Bump Natural Pain Relief Gel from Lot D54947.
- Dispose of the product or return it to the retailer per the distributor’s instructions.
- Check your bottle’s lot number (D54947) and expiry date (4/30/2028) to confirm if it is affected.
- Contact CA BOTANA International, Inc. or 1Beauty US LLC for disposal instructions or more information, or visit the FDA recall page.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.