Device recall
Z-1898-2017: Wingman 35 Crossing Catheter, 65cm, Model Numbers: WGM35065US WGM35065CE…
FDA device recall · Class I · ReFlow Medical
Key facts
| Recall number (Z-number) | Z-1898-2017 |
|---|---|
| Recall event | 76821 |
| Product | Wingman 35 Crossing Catheter, 65cm, Model Numbers: WGM35065US WGM35065CE WGM35090US WGM35090CE WGM35135US WGM35135CE |
| Product code | DQY |
| Recalling firm | ReFlow Medical |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 6, 2017 |
| 510(k) numbers | K141547 |
| FEI number | 3008789872 |
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