Device recall
Z-1623-2016: Distal Femoral Replacement (patient specific, custom made orthopedic implant…
FDA device recall · Class II · Stanmore Implants Worldwide Ltd.
Key facts
| Recall number (Z-number) | Z-1623-2016 |
|---|---|
| Recall event | 73856 |
| Product | Distal Femoral Replacement (patient specific, custom made orthopedic implant device). PIN 19960 |
| Product code | JWH |
| Recalling firm | Stanmore Implants Worldwide Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2017 |
| FEI number | 3004105610 |
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