Device recall
Z-2154-2020: Knee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-2154-2020 |
|---|---|
| Recall event | 85524 |
| Product | Knee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28 MM; 184764 Knees Vanguard Knee System, Series-A Standard Patella, 31 MM Product Usage: Knee prosthesis |
| Product code | JWH |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2021 |
| 510(k) numbers | K040770 |
| FEI number | 1825034 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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