Device recall
Z-1456-2019: CBS high, countersink, cannulated, round-shaft, Item Number 503004342
FDA device recall · Class II · Zimmer GmbH
Key facts
| Recall number (Z-number) | Z-1456-2019 |
|---|---|
| Recall event | 82642 |
| Product | CBS high, countersink, cannulated, round-shaft, Item Number 503004342 |
| Product code | HWW |
| Recalling firm | Zimmer GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 11, 2020 |
| FEI number | 3005233524 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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