FDA Drugs recall ·
DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz recall
- Recall number
- D-0602-2026
- Date
- (initiated May 21, 2026)
- Company / brand
- Keystone Industries
480 S Democrat Rd, Gibbstown, NJ, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 150 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Manufactured for and Distributed by Dental Health Products, Inc, 2614 North Sugar Bush Road, New Franken, WI 54229. NDC 69634-020-30
Why was it recalled?
Defective container:may contain bottles with incomplete seals
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
BNZ-001921, EXP 04/15/2029
Distribution
Nationwide in the USA
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0602-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.