FDA recall D-0605-2026

Keystone Industries · Class II · drug

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 for recall

Defective container:may contain bottles with incomplete seals

Distribution

Nationwide in the USA

Key facts

Status: Ongoing
Initiation date: 2026-05-21
Report date: 2026-06-24
Voluntary/Mandated: Voluntary: Firm initiated
Location: Gibbstown, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0605-2026