Device recall
Z-0244-2022: Torque Limiting Adaptor, AO Connect, 4 N-m, part #027-203, reusable, a component…
FDA device recall · Class II · Laboratoires Bodycad, Inc.
Key facts
| Recall number (Z-number) | Z-0244-2022 |
|---|---|
| Recall event | 88878 |
| 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. |
| Product code | LXH |
| Recalling firm | Laboratoires Bodycad, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 4, 2023 |
| FEI number | 3012086398 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database