Device recall
Z-2566-2014: Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa…
FDA device recall · Class II · Biomet Microfixation, LLC
Key facts
| Recall number (Z-number) | Z-2566-2014 |
|---|---|
| Recall event | 67547 |
| Product | Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to functionally reconstruct a diseased and/or damaged temporomandibular joint. The Total TMJ replacement system is a… |
| Product code | LZD |
| Recalling firm | Biomet Microfixation, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 3, 2014 |
| PMA numbers | P020016 |
| FEI number | 1032347 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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