Device recall
Z-3299-2024: Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with…
FDA device recall · Class II · ARROW INTERNATIONAL Inc.
Key facts
| Recall number (Z-number) | Z-3299-2024 |
|---|---|
| Recall event | 95228 |
| Product | Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-BW1; (2) Arrow Arterial Access Tray with 0.021" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-CK; (3) Arrow Arterial Access Kit, .025 inch dia… |
| Product code | DQX |
| Recalling firm | ARROW INTERNATIONAL Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K810675, K914531 |
| FEI number | 3013162291 |
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