Device recall
Z-0280-06: Stainless Steel Greenfield Vena Cava Filter with 12 Fr / 4,0 mm FlexCarrier…
FDA device recall · Class I · Boston Scientific
Key facts
| Recall number (Z-number) | Z-0280-06 |
|---|---|
| Recall event | 34134 |
| Product | Stainless Steel Greenfield Vena Cava Filter with 12 Fr / 4,0 mm FlexCarrier Capsule. For Femoral Vein Introduction Only. Order No. 50-501. Sterile EO. Single Use Only. Read Instructions for Use before using this device. Distributed in USA by: Boston Scientific Corporation, One Boston Scientific… |
| Product code | DTK |
| Recalling firm | Boston Scientific |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 2, 2007 |
| 510(k) numbers | K964284 |
| 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