Device recall
Z-1735-2020: Percuflex Plus Ureteral Stent Set 7FX24CM with.035 Sensor UPN: M006175272080…
FDA device recall · Class II · Boston Scientific
Key facts
| Recall number (Z-number) | Z-1735-2020 |
|---|---|
| Recall event | 85227 |
| Product | Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor UPN: M006175272080 (edited 1/13/2021) |
| Product code | EZB |
| Recalling firm | Boston Scientific |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3005099803 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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