Device recall
Z-0723-2019: Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-0723-2019 |
|---|---|
| Recall event | 81665 |
| Product | Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm, Reference # CS-12402 The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access… |
| Product code | DQY |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 4, 2020 |
| 510(k) numbers | K862056 |
| 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