FDA Drugs recall ·
Dr. Bump Natural Pain Relief Gel, Menthol 5%… recall
- Recall number
- D-0196-2026
- Date
- (initiated October 10, 2025)
- Company / brand
- CA BOTANA International, Inc.
9505 Chesapeake Dr, San Diego, CA, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 4890 bottles
- Hazard tags
- Manufacturing practices (cGMP)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it recalled?
CGMP Deviations
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot D54947, exp 4/30/2028
Distribution
CA, CO, FL, PR, WA
States: California Colorado Florida Puerto Rico Washington
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0196-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.