Keystone Industries: Purelife, Topical Anesthetic Gel, Benzocaine 20%
Recall Summary PureLife Topical Anesthetic Gel (Benzocaine 20%, 1 oz strawberry flavor) is being recalled nationwide because some bottles may have incomplete seals. The product was manufactured for Pure Life, LLC in Carson, California and distributed across all U.S. states.
- Recalling firm
- Keystone Industries
- Product
- PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for Pure Life, LLC, Manufactured for PureLife LLC., Carson, CA 90810. NDC 68987-001-30
- Reason
- Defective container:may contain bottles with incomplete seals
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-05-21
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide in the USA
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/bfccf161-82ad-4ba7-972c-5d84b725063b