DHP Topical Anesthetic Gel recall — Keystone Industries
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries
Affected product: DHP Topical Anesthetic Gel
Official ID D-0602-2026 · Official record ↗
Notice names this product. Keystone Industries’s DHP Topical Anesthetic Gel is named in FDA Class II recall D-0602-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Defective container:may contain bottles with incomplete seals Identifying details: BNZ-001921, EXP 04/15/2029. Units affected: 150 units. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
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
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries
Affected product: DHP Topical Anesthetic Gel
Official ID D-0602-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.