Device recall
Z-0527-2022: PIVO Blood Collection Device 20G, REF: 202-0005
FDA device recall · Class II · Velano Vascular
Key facts
| Recall number (Z-number) | Z-0527-2022 |
|---|---|
| Recall event | 89185 |
| Product | PIVO Blood Collection Device 20G, REF: 202-0005 |
| Product code | JKA |
| Recalling firm | Velano Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 31, 2023 |
| 510(k) numbers | K193569 |
| FEI number | 1710034 |
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