Device recall
Z-2517-2018: 2M insert 15degree for MUTARS RS cup and LUMiC TiN orthopedic hip implant…
FDA device recall · Class II · IMPLANTCAST GMBH
Key facts
| Recall number (Z-number) | Z-2517-2018 |
|---|---|
| Recall event | 80498 |
| Product | 2M insert 15degree for MUTARS RS cup and LUMiC TiN orthopedic hip implant acetabular component. Size 38/39 mm REF number 02423839 Size 42/44 mm REF number 02424244 Size 44/48 mm REF number 02424448 Size 46/52 mm REF number 02424652 |
| Product code | LZO |
| Recalling firm | IMPLANTCAST GMBH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 1, 2020 |
| FEI number | 3012523063 |
At a glance
- None 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