Device recall
Z-1818-2019: Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1818-2019 |
|---|---|
| Recall event | 82865 |
| Product | Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS |
| Product code | PND |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2021 |
| 510(k) numbers | K161313 |
| FEI number | 3015859709 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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