X-Jow Pain Gel recalled over manufacturing violations
- Recall date
- May 25, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Shadow Holdings DBA Bocchi Labs recalls X-Jow (menthol USP) Pain Gel, 1.25%, packaged in a) 4 oz. (113g) bottles (UPC 850547 00502 6) and b) 8 oz. (226g) bottl…
- Recall number
- D-0858-2018
- FDA classification
- Class II
- Brand / firm
- Shadow Holdings DBA Bocchi Labs
- Sold / distributed
- Nationwide in the USA
Why it was recalled
CGMP Deviations: products may be contaminated with bacteria.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What 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.
Get recall alerts
Free email alert whenever Shadow Holdings DBA Bocchi Labs has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Shadow Holdings DBA Bocchi Labs