Device recall
Z-1828-2021: VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen…
FDA device recall · Class III · MICROVENTION INC.
Key facts
| Recall number (Z-number) | Z-1828-2021 |
|---|---|
| Recall event | 88024 |
| Product | VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature. |
| Product code | DQY |
| Recalling firm | MICROVENTION INC. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 16, 2024 |
| 510(k) numbers | K192135 |
| FEI number | 3013556777 |
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