PlainRecalls
FDA Drug Moderate Class II Terminated

X-Jow (menthol USP) Pain Gel, 1.25%, packaged in a) 4 oz. (113g) bottles (UPC 850547 00502 6) and b) 8 oz. (226g) bottles (UPC 8 50547 00503 3, Distributed by Herb-X Solutions, Inc., 3838 West Burbank Blvd., Burbank CA 91505.

Reported: June 20, 2018 Initiated: May 25, 2018 #D-0858-2018

Product Description

X-Jow (menthol USP) Pain Gel, 1.25%, packaged in a) 4 oz. (113g) bottles (UPC 850547 00502 6) and b) 8 oz. (226g) bottles (UPC 8 50547 00503 3, Distributed by Herb-X Solutions, Inc., 3838 West Burbank Blvd., Burbank CA 91505.

Reason for Recall

CGMP Deviations: products may be contaminated with bacteria.

Details

Units Affected
12,252 bottles
Distribution
Nationwide in the USA
Location
Santa Clarita, CA

Frequently Asked Questions

What product was recalled?
X-Jow (menthol USP) Pain Gel, 1.25%, packaged in a) 4 oz. (113g) bottles (UPC 850547 00502 6) and b) 8 oz. (226g) bottles (UPC 8 50547 00503 3, Distributed by Herb-X Solutions, Inc., 3838 West Burbank Blvd., Burbank CA 91505.. Recalled by Shadow Holdings DBA Bocchi Labs. Units affected: 12,252 bottles.
Why was this product recalled?
CGMP Deviations: products may be contaminated with bacteria.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 20, 2018. Severity: Moderate. Recall number: D-0858-2018.