# FDA recall Z-0853-2022

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2022-03-10.

## Product

EasyFuse Dynamic Compression System Instrument Pack

## Reason for recall

The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.

## Distribution

US distribution to Florida, North Carolina, Ohio, and Texas

## Key facts

- **Recall number:** Z-0853-2022
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-03-10
- **Report date:** 2022-04-06
- **Termination date:** 2026-04-01

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0853-2022

## Citation

> AI Analytics. FDA recall Z-0853-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0853-2022. Source: US FDA. Licensed CC0.

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