Device recall
Z-0114-2017: VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27…
FDA device recall · Class II · Sequent Medical Inc
Key facts
| Recall number (Z-number) | Z-0114-2017 |
|---|---|
| Recall event | 75211 |
| Product | VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of non-liquid interventional devices (such as stents/flow diverters) and infusion of diagnostic (such as contrast media) or therapeutic agents into the neuro, peripheral, and coronary… |
| Product code | KRA |
| Recalling firm | Sequent Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2017 |
| 510(k) numbers | K132652 |
| FEI number | 3008423090 |
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