Device recall
Z-0349-05: NeoPICC 1.9 FR Catheter. Percutaneous Implanted long term intravascular…
FDA device recall · Class I · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-0349-05 |
|---|---|
| Recall event | 30528 |
| Product | NeoPICC 1.9 FR Catheter. Percutaneous Implanted long term intravascular catheter. The product is shipped in cases of 5 units. Catalog numbers S1PIC1.9-S, S1PIC1.9-N, S1PIC1.9-SMK, and S1PIC1.9-C. |
| Product code | LJS |
| Recalling firm | Arrow International Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 14, 2006 |
| 510(k) numbers | K970434 |
| FEI number | 3015859709 |
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