Device recall
Z-2096-2016: AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203
FDA device recall · Class I · Stryker Sustainability Solutions
Key facts
| Recall number (Z-number) | Z-2096-2016 |
|---|---|
| Recall event | 74301 |
| Product | AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203 |
| Product code | DQO |
| Recalling firm | Stryker Sustainability Solutions |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 19, 2016 |
| 510(k) numbers | K001578 |
| FEI number | 3009350690 |
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