# FDA recall D-0858-2018

> **Shadow Holdings DBA Bocchi Labs** · Class II · drug recall initiated 2018-05-25.

## Product

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.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0858-2018
- **Recalling firm:** Shadow Holdings DBA Bocchi Labs
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-05-25
- **Report date:** 2018-06-20
- **Termination date:** 2019-08-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Santa Clarita, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0858-2018

## Citation

> AI Analytics. FDA recall D-0858-2018. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0858-2018. Source: US FDA. Licensed CC0.

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