US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 16, 2018 (8 years ago)

BeeGentle Honey Flavored Topical Anesthetic, Active ingredient Benzocaine 20%. Packaged…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP violations noted during the firm's most recent inspection.

What was recalled

BeeGentle Honey Flavored Topical Anesthetic, Active ingredient Benzocaine 20%. Packaged in: a) Introductory Kit. Net Qty 3-3cc preloaded syringes. . NDC# 1406000203 UPC 8 72320 00074 5 b) Bulk Kit Net Qty 30mL, NDC# 1406000202, UPC 8 72320 00076 9. Manufactured by CAO (China) Medical Equipment Co. Ltd. for CAO Group, Inc. 4628 West Skyhawk Drive, West Jordan, UT 84084

Recalling firm
CAO Group, Inc.
Origin
UT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0292-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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