Device recall
Z-2183-2018: Vanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in…
FDA device recall · Class II · Zimmer Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-2183-2018 |
|---|---|
| Recall event | 80172 |
| Product | Vanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in knee joint replacement procedures. |
| Product code | JWH |
| Recalling firm | Zimmer Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 2019 |
| 510(k) numbers | K113550, K171054 |
| 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