Device recall
Z-0082-04: Arrow Howes multi-lumen central venous catheterization kit 7 Fr x 20 cm
FDA device recall · Class III · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-0082-04 |
|---|---|
| Recall event | 27415 |
| Product | Arrow Howes multi-lumen central venous catheterization kit 7 Fr x 20 cm |
| Product code | KZH |
| Recalling firm | Arrow International Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 5, 2004 |
| 510(k) numbers | K900263 |
| FEI number | 3015859709 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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