Device recall
Z-0509-2015: Total Temporomandibular Joint Replacement System- 45mm Lft Narrow Ti Mand
FDA device recall · Class II · Biomet Microfixation, LLC
Key facts
| Recall number (Z-number) | Z-0509-2015 |
|---|---|
| Recall event | 69644 |
| Product | Total Temporomandibular Joint Replacement System- 45mm Lft Narrow Ti Mand |
| Product code | LZD |
| Recalling firm | Biomet Microfixation, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 4, 2017 |
| PMA numbers | P020016 |
| FEI number | 1032347 |
At a glance
- None Linked 510(k)s
- 10–99 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