Device recall
Z-2240-2016: TSP Hip Fracture Plating System device, fixation, proximal femoral, implant The…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-2240-2016 |
|---|---|
| Recall event | 74576 |
| Product | TSP Hip Fracture Plating System device, fixation, proximal femoral, implant The Biomet Hip Fracture Plating Systems are indicated for use in the open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures and intertrochanteric fractures… |
| Product code | JDO |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 20, 2017 |
| 510(k) numbers | K140018 |
| FEI number | 1825034 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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