FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass II · Drug · Recalled June 24, 2026

PureLife recall — Keystone Industries

Hazard: Defective container:may contain bottles with incomplete seals

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
D-0605-2026
Brand
Keystone Industries
Classification
Class II
Units affected
450 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

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

Affected products

Companies & origin

Recalling firm location
Gibbstown, NJ, United States
Firm address
480 S Democrat Rd, 08027-1239

Identifying details (verbatim from the notice)

Product codes / lots
BNZ-001921, EXP 04/15/2029
Distribution
Nationwide in the USA
Firm notified the public via
Letter
FDA event ID
99076
Recall initiated
May 21, 2026
FDA classified
June 18, 2026
FDA report date
June 24, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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