Recalling firm
Keystone Industries
Product type
Drug
Status
Ongoing
Report date
2026-06-24
Distribution
Nationwide in the USA
Firm state
NJ
Product quantity
450 units
Initiated by
Voluntary: Firm initiated
Reason for recall
Defective container:may contain bottles with incomplete seals
Product description
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
Code / lot info
BNZ-001921, EXP 04/15/2029
Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.