Device recall
Z-2556-2019: Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-2556-2019 |
|---|---|
| Recall event | 83593 |
| Product | Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins. |
| Product code | DYB |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 29, 2020 |
| FEI number | 3015859709 |
At a glance
- None 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