Device recall
Z-2050-2021: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit cup…
FDA device recall · Class II · IMPLANTCAST GMBH
Key facts
| Recall number (Z-number) | Z-2050-2021 |
|---|---|
| Recall event | 88047 |
| Product | EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit cup cementless 46mm dia incl. central hole cover; 02200048 /EcoFit cup cementless 48mm dia incl. central hole cover; 02200050 /EcoFit cup cementless 50mm dia incl. central hole cover; 02200052 /EcoFit cup cementless 52mm dia… |
| Product code | LZO |
| Recalling firm | IMPLANTCAST GMBH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 18, 2022 |
| 510(k) numbers | K163577 |
| FEI number | 3012523063 |
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