Device recall
Z-1799-2019: Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1799-2019 |
|---|---|
| Recall event | 82865 |
| Product | Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A |
| Product code | LJS |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2021 |
| 510(k) numbers | K132133 |
| 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