Device recall
Z-1132-2015: CoCr Femoral Head - A modular head component is used in conjunction with a…
FDA device recall · Class II · Zimmer Gmbh
Key facts
| Recall number (Z-number) | Z-1132-2015 |
|---|---|
| Recall event | 70401 |
| Product | CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of the proximal femur in total hip arthroplasty. |
| Product code | LPH |
| Recalling firm | Zimmer Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 23, 2015 |
| 510(k) numbers | K993259 |
| FEI number | 3005233524 |
At a glance
- 1–9 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