# FDA recall Z-0244-2022

> **Laboratoires Bodycad, Inc.** · Class II · device recall initiated 2021-07-02.

## Product

Torque Limiting Adaptor, AO Connect, 4 N-m, part #027-203, reusable, a component of the Bodycad Fine Osteotomy Implant and Disposable Instrumentation Tray, part #025-004.

## Reason for recall

There is a risk of breakage of the torque limiting adaptor if used counterclockwise and it must not be used with a power tool due to no test data validating this use.

## Distribution

Distribution was made to CO, MI, and NY.  Foreign distribution was made to Canada and the United Kingdom.  There was no military/government distribution.

## Key facts

- **Recall number:** Z-0244-2022
- **Recalling firm:** Laboratoires Bodycad, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-02
- **Report date:** 2021-11-24
- **Termination date:** 2023-01-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Quebec, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0244-2022

## Citation

> AI Analytics. FDA recall Z-0244-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0244-2022. Source: US FDA. Licensed CC0.

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