By the pharmaranks editorial team·Reviewed against the FDA (openFDA) sources·Updated Jun 24, 2026·How we research
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
Defective container:may contain bottles with incomplete seals
Details
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
Recalling company
Keystone Industries
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Nationwide in the USA
Initiated
May 21, 2026
FDA report date
Jun 24, 2026
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.