BeeGentle Honey Flavored Topical Anesthetic — Class II drug recall D-0292-2019
Terminated recall by CAO Group, Inc., reported 2018-12-19, distributed nationwide. cGMP violations noted during the firm's most recent inspection.
| Recall number | D-0292-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CAO Group, Inc., West Jordan, UT, United States |
| Recall initiated | 2018-11-16 |
| Classified | 2018-12-11 |
| Reported by FDA | 2018-12-19 |
| Terminated | 2020-02-27 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00872320000745, 00872320000769 |
| Expiration dates | 2018-11-02, 2019-03-23, 2019-05-24, 2019-11-16, 2020-01-09, 2020-03-19 |
Product
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
Reason for recall
cGMP violations noted during the firm's most recent inspection.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0292-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.