FDA-Drug2026-06-24Class IIPACKAGING DEFECT
PureLife topical anesthetic gel recalled for defective container seals
OTHERNationwide distribution
PureLife benzocaine gel recalled for defective bottle seals
PureLife topical anesthetic gel (benzocaine 20%, 1 oz) may contain bottles with incomplete seals. This could allow the product to leak or become contaminated. About 450 units were distributed nationwide.
- Check your PureLife topical anesthetic gel bottle for signs of leakage or damage.
- Do not use the product if the seal appears incomplete or broken.
- Contact your pharmacy or retailer for a replacement or refund.
Hazard
Defective container:may contain bottles with incomplete seals
Sold states
Nationwide in the USA
Affected count
450 units
Manufactured in
480 S Democrat Rd, Gibbstown, NJ, United States
Products
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
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0605-2026More Keystone Industries recalls
- FDA-Drug2026-06-24DHP Topical Anesthetic Gel (Benzocaine 20%) recalled for defective container seals
- FDA-Drug2026-06-24Quala topical anesthetic gel recalled for incomplete bottle seals
- FDA-Drug2026-06-24Dental City Benzocaine 20% topical anesthetic gel recalled for incomplete bottle seals
- FDA-Drug2026-06-24Burkhart topical anesthetic gel recalled for defective bottles with incomplete seals
- FDA-Drug2026-06-24Safco SensiCaine-Ultra benzocaine gel recalled for incomplete bottle seals
Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief