Keystone Industries: Drug Recall

Recall #D-0148-2025 · 11/14/2024

Class II: Risk

Recall Details

Recall Number
D-0148-2025
Classification
Class II
Product Type
Drug
Recalling Firm
Keystone Industries
Status
Ongoing
Date Initiated
11/14/2024
Location
Gibbstown, NJ, United States
Voluntary/Mandated
Voluntary: Firm initiated

Reason for Recall

CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

Product Description

Henry Schein, Benzo-Jel, Topical Anesthetic Gel, 20% Benzocaine, 1 fl. oz. (29.6 mL), Distributed by Henry Schein, Melville, NY 11747, For Professional Use Only,

Distribution Pattern

Nationwide in the USA and Canada, Dominican Republic, El Salvador, Honduras, and Qatar.

Other Recalls by Keystone Industries

View all recalls by Keystone Industries →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.