Device recall
Z-2156-2020: Knee Products: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-2156-2020 |
|---|---|
| Recall event | 85524 |
| Product | Knee Products: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model (01)00841036226534(17)220111(10)735550 Product Usage: Knee prosthesis |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2021 |
| FEI number | 1825034 |
At a glance
- None Linked 510(k)s
- 10–99 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