Dental City recalled over manufacturing violations
- Recall date
- November 14, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Keystone Industries recalls Dental City, Topical Anesthetic Gel, Benzocaine 20%, Net Content: 1 oz. (30 ml), Gluten Free, Manufactured for: Dental…
- Recall number
- D-0140-2025
- FDA classification
- Class II
- Brand / firm
- Keystone Industries
- Sold / distributed
- Nationwide in the USA and Canada, Dominican Republic, El Salvador, Honduras, and Qatar.
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Dental City, Topical Anesthetic Gel, Benzocaine 20%, Net Content: 1 oz. (30 ml), Gluten Free, Manufactured for: Dental City, Green Bay, WI 54311, dentalcity.com.
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