Device recall
Z-0300-06: Titanium Greenfield Vena Cava Filter with 12 Fr./4,0 mm Introducer System…
FDA device recall · Class II · Boston Scientific Scimed
Key facts
| Recall number (Z-number) | Z-0300-06 |
|---|---|
| Recall event | 32889 |
| Product | Titanium Greenfield Vena Cava Filter with 12 Fr./4,0 mm Introducer System. Catalog no. M001503010. Sterile EO. Single Use Only. Manufacturer: Boston Scientific Cork Ltd., Business and Technology Park, Model Farm Rd., Cork, Ireland. Distributed in USA by: Boston Scientific Corporation, One Boston… |
| Product code | DTK |
| Recalling firm | Boston Scientific Scimed |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 9, 2006 |
| 510(k) numbers | K901659 |
| FEI number | 3002095335 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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