Device recall
Z-2481-2019: OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component ApeX-LNK…
FDA device recall · Class II · OMNIlife science Inc.
Key facts
| Recall number (Z-number) | Z-2481-2019 |
|---|---|
| Recall event | 83528 |
| Product | OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component ApeX-LNK crosslinked Acetabular Insert, 10 deg hood; Product Code : H5-54840 |
| Product code | LPH |
| Recalling firm | OMNIlife science Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 24, 2020 |
| 510(k) numbers | K100555 |
| FEI number | 3008342029 |
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