Device recall
Z-0127-2016: 4FR Single Lumen Pressure Injectable PICC; intravascular therapeutic catheter…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-0127-2016 |
|---|---|
| Recall event | 72244 |
| Product | 4FR Single Lumen Pressure Injectable PICC; intravascular therapeutic catheter, for long-term use greater than 30 days. |
| Product code | LJS |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2020 |
| 510(k) numbers | K061289, K073451 |
| 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