# FDA recall Z-0392-2022

> **Wright Medical Technology Inc** · Class II · device recall initiated 2021-12-03.

## Product

Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.

## Reason for recall

The incorrect product is contained in the packaging.

## Distribution

Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV.  The countries of  Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.

## Key facts

- **Recall number:** Z-0392-2022
- **Recalling firm:** Wright Medical Technology Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-12-03
- **Report date:** 2021-12-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arlington, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0392-2022

## Citation

> AI Analytics. FDA recall Z-0392-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0392-2022. Source: US FDA. Licensed CC0.

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