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Class II: temporary or reversible health riskTerminated

CAO Group BeeGentle Honey Flavored Topical Anesthetic Recall

BeeGentle Honey Flavored Topical Anesthetic, Active ingredient Benzocaine 20%

CAO Group, Inc. · West Jordan, UT

Risk level
Class II
Reported by FDA
Dec 19, 2018
Recall ID
D-0292-2019
Check your lot numberHow we source this data

Summary

CAO Group recalled BeeGentle Honey Flavored Topical Anesthetic starting Nov 16, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0292-2019 on Dec 19, 2018. Reason: cGMP violations noted during the firm's most recent inspection. Status: Terminated.

Why it was recalled

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

Product description

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

Lot numbers, UPCs & expiration codes

Lots #: a) 110216, EXP 11/02/18; 170524, EXP 5/24/2019; 171116, EXP 11/16/2019; 180319, EXP 3/19/2020; b)110216, EXP 11/02/2018; 170323, EXP 3/23/2019; 180109, EXP 1/09/2020

Where it was sold

Nationwide in the US

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0292-2019
Classification
Class II
Status
Terminated
Recall initiated
Nov 16, 2018
FDA report date
Dec 19, 2018
Quantity
803 units (400 kit and 403 30 ml bottles)
Recall type
Voluntary: Firm initiated
Recalling firm
CAO Group, Inc.

Original FDA data

Every field from FDA enforcement report D-0292-2019, exactly as published.

Show all FDA fields
City
West Jordan
State
UT
Status
Terminated
Country
United States
Event ID
81556
Address
4628 W Skyhawk Dr
Code information
Lots #: a) 110216, EXP 11/02/18; 170524, EXP 5/24/2019; 171116, EXP 11/16/2019; 180319, EXP 3/19/2020; b)110216, EXP 11/02/2018; 170323, EXP 3/23/2019; 180109, EXP 1/09/2020
Postal code
84084-4501
Report date
Dec 19, 2018
Product type
Drugs
Recall number
D-0292-2019
Classification
Class II
Recalling firm
CAO Group, Inc.
Product quantity
803 units (400 kit and 403 30 ml bottles)
Termination date
Feb 27, 2020
Reason for recall
cGMP violations noted during the firm's most recent inspection.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Nationwide in the US
Recall initiation date
Nov 16, 2018
Initial firm notification
Letter
Center classification date
Dec 11, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0292-2019, published Dec 19, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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