Device recall
Z-0895-06: Boston Scientific brand Pivot Steerable Microcatheter, 1.9F/2.4F, Catalog #…
FDA device recall · Class II · Boston Scientific Target
Key facts
| Recall number (Z-number) | Z-0895-06 |
|---|---|
| Recall event | 35301 |
| Product | Boston Scientific brand Pivot Steerable Microcatheter, 1.9F/2.4F, Catalog #: 1721, Universal Product Number: M00317210, Product is Manufactured by: Boston Scientific - Precision Vascular, 2405 West Orton Cir. West Valley City, UT 84119 |
| Product code | KRA |
| Recalling firm | Boston Scientific Target |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2006 |
| 510(k) numbers | K050630 |
| FEI number | 2939204 |
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