Device recall
Z-2529-2017: Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath…
FDA device recall · Class II · Creganna Medical Devices
Key facts
| Recall number (Z-number) | Z-2529-2017 |
|---|---|
| Recall event | 77406 |
| Product | Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USTMCA85200 |
| Product code | DYB |
| Recalling firm | Creganna Medical Devices |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 29, 2018 |
| 510(k) numbers | K131079 |
| FEI number | 3004193842 |
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