Device recall
Z-1095-05: ChemoSite Implantable venous access sytem with printed Polyurethane Catheter and…
FDA device recall · Class II · United States Surgical Corporation
Key facts
| Recall number (Z-number) | Z-1095-05 |
|---|---|
| Recall event | 32569 |
| Product | ChemoSite Implantable venous access sytem with printed Polyurethane Catheter and 9 French Introducer Kit Catalog Number: 120045 |
| Product code | LJS |
| Recalling firm | United States Surgical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 14, 2010 |
| 510(k) numbers | K902135 |
| FEI number | 1219930 |
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