Device recall
Z-2338-2017: Arrow Pressure Injectable PICC Kit Catheter, Intravascular, Therapeutic…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-2338-2017 |
|---|---|
| Recall event | 77232 |
| Product | Arrow Pressure Injectable PICC Kit Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days The Arrow Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling. |
| Product code | LJS |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 17, 2018 |
| 510(k) numbers | K061289 |
| FEI number | 3015859709 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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