Device recall
Z-1941-2024: The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip…
FDA device recall · Class II · Stryker Neurovascular
Key facts
| Recall number (Z-number) | Z-1941-2024 |
|---|---|
| Recall event | 94543 |
| Product | The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and pre-shaped versions. The outside diameters of the guidewires are 0.014 in. The guidewires are compatible with existing microcatheters used in common procedures such as those used in… |
| Product code | DQX |
| Recalling firm | Stryker Neurovascular |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K053268 |
| FEI number | 3008853977 |
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