BeeGentle Honey Flavored Topical Anesthetic recalled over manufacturing violations
- Recall date
- November 16, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- CAO Group, Inc. recalls BeeGentle Honey Flavored Topical Anesthetic, Active ingredient Benzocaine 20%. Packaged in: a) Introductory Kit. Net Qt…
- Recall number
- D-0292-2019
- FDA classification
- Class II
- Brand / firm
- CAO Group, Inc.
- Sold / distributed
- Nationwide in the US
Why it was recalled
cGMP violations noted during the firm's most recent inspection.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
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
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