Device recall
Z-2260-2024: Curved, super elastic cement delivery needle that passes through the cannula in…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2260-2024 |
|---|---|
| Recall event | 94755 |
| Product | Curved, super elastic cement delivery needle that passes through the cannula in a straight configuration and enters the vertebral body in a curved configuration. This provides physicians with the ability to inject bone cement into multiple different areas through a single point of access in the… |
| Product code | OAR |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3015967359 |
At a glance
- None Linked 510(k)s
- 1–9 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