Torque Limiting Adaptor — Class II medical device recall Z-0244-2022
Terminated recall by Laboratoires Bodycad, Inc., reported 2021-11-24, distributed in CO, MI, NY. There is a risk of breakage of the torque limiting adaptor if used counterclockwise and it must not be used wi
| Recall number | Z-0244-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Laboratoires Bodycad, Inc., Quebec, N/A, Canada |
| Recall initiated | 2021-07-02 |
| Classified | 2021-11-17 |
| Reported by FDA | 2021-11-24 |
| Terminated | 2023-01-04 |
| Distributed | CO, MI, NY |
| Countries outside the US | CA, GB |
| Quantity | 10 in |
| Reason classes | device malfunction |
| Lot numbers | SB000251, SB000252, SB000253, SB000254, SB000259, SB000261, SB000263, SB000264, SB000272, SB000273, SB000430 |
| Model numbers | 025-004, 027-203 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0244-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.