Device recall
Z-1011-2018: Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee…
FDA device recall · Class II · Zimmer Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1011-2018 |
|---|---|
| Recall event | 79250 |
| Product | Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty |
| Product code | MBH |
| Recalling firm | Zimmer Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2018 |
| 510(k) numbers | K113550 |
| FEI number | 1825034 |
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