Device recall
Z-0849-2012: Natural-Knee II Durasul All-Poly Patella, Size 1, 7mm The Zimmer Natural-Knee II…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0849-2012 |
|---|---|
| Recall event | 60858 |
| Product | Natural-Knee II Durasul All-Poly Patella, Size 1, 7mm The Zimmer Natural-Knee II Durasul Patella product is a semi-constrained total knee prosthesis consisting of four anatomically designed components: the femoral, tibial, articular surface, and patellar prosthesis. The all-polyethylene patella is… |
| Product code | JWH |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 21, 2015 |
| 510(k) numbers | K002335 |
| FEI number | 1000220733 |
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