Device recall
Z-1130-2014: FMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO…
FDA device recall · Class II · Djo Surgical
Key facts
| Recall number (Z-number) | Z-1130-2014 |
|---|---|
| Recall event | 67468 |
| Product | FMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO Surgical hip systems. It is used with an acetabular shell to replicate the kinematics of a natural hip. |
| Product code | LPH |
| Recalling firm | Djo Surgical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 1, 2014 |
| 510(k) numbers | K072154 |
| FEI number | 1000116912 |
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