Device recall
Z-0630-2007: Vaxcel Implantable Vascular Access System - Titanium Mini-Port with PASV Valve…
FDA device recall · Class II · Boston Scientific Corp
Key facts
| Recall number (Z-number) | Z-0630-2007 |
|---|---|
| Recall event | 37442 |
| Product | Vaxcel Implantable Vascular Access System - Titanium Mini-Port with PASV Valve and 8F Polyurethane Catheter, REF/Catalog No. 45-215, UPN/Material No. M001452150, |
| Product code | LJT |
| Recalling firm | Boston Scientific Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 26, 2007 |
| 510(k) numbers | K030083 |
| FEI number | 3017892510 |
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