Device recall
Z-0255-04: Arrow A Port with Attachable Silicone Rubber Catheters Implantable Vascular…
FDA device recall · Class III · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-0255-04 |
|---|---|
| Recall event | 27681 |
| Product | Arrow A Port with Attachable Silicone Rubber Catheters Implantable Vascular Access System (Product # AP-01510) . Product # AP-01510 kit contains 1 implantable titanium port, 2 attachable silicone rubber catheters (8.4 Fr. x 75 cm and 9.6 Fr x 75 cm) straight non-coring needle, patient ID card and… |
| Product code | DYB |
| Recalling firm | Arrow International Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 12, 2004 |
| 510(k) numbers | K921475, K933316, K934802 |
| FEI number | 3010532612 |
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