FDAClass II · Drug · Recalled June 24, 2026

Pearson Quality Topical Anesthetic Gel (20% Benzocaine) 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-0600-2026
Brand: Keystone Industries
Classification: Class II
Units affected: 900 units
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Contents: 1 oz (3o g), Manufactured for: Pearson Dental Supply Inc., Sylmar, CA 91342 USA, NDC 43305-0009-3.

Affected products

Pearson Quality Topical Anesthetic Gel (20% Benzocaine)

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-001917, Exp 04/01/2029
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 24, 2026 at 12:00 AM UTC.

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