Device recall
Z-2327-2017: Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-2327-2017 |
|---|---|
| Recall event | 77232 |
| Product | Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features wire, guide, catheter The Arrow Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels |
| Product code | DQX |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 17, 2018 |
| 510(k) numbers | K810675 |
| FEI number | 3015859709 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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