Device recall
Z-1336-2018: ARROWg+ard Blue Two-Lumen Hemodialysis Catheterization Kit for High Volume…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1336-2018 |
|---|---|
| Recall event | 79512 |
| Product | ARROWg+ard Blue Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions (1) Part Number (PN): CDC-22122-1A; (2) PN: CDC-25122-1A; (3) PN: CDC-25142-1A; (4) CDC-26142-1A |
| Product code | MPB |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 27, 2020 |
| 510(k) numbers | K993933 |
| FEI number | 3015859709 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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