Device recall
Z-0207-2016: ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-0207-2016 |
|---|---|
| Recall event | 72463 |
| Product | ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit ARROW Advantage5 Pressure Injectable PICC Kit Arrow Pressure Injectable Arrow PICC powered by Arrow VPS Stylet ARROW Pressure Injectable JACC with Chlorag+ard Technology For short-term or long-term peripheral access to the… |
| Product code | LJS |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 9, 2017 |
| 510(k) numbers | K112896, K113277, K121941, K122854, K132133 |
| 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