Device recall
Z-1035-03: 9 French Super Arrow-Flex Percutaneous Sheath Introducer Kit with Arrowg and…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1035-03 |
|---|---|
| Recall event | 26680 |
| Product | 9 French Super Arrow-Flex Percutaneous Sheath Introducer Kit with Arrowg and Blue Antimicrobial Surface Sheath |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 2, 2004 |
| 510(k) numbers | K940079 |
| FEI number | 3015859709 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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