Device recall
Z-1013-2011: VAD Kit Reorder DT8915, Sterile, Centurion Medical Products Corp. Williamston…
FDA device recall · Class II · Centurion Medical Products
Key facts
| Recall number (Z-number) | Z-1013-2011 |
|---|---|
| Recall event | 57661 |
| Product | VAD Kit Reorder DT8915, Sterile, Centurion Medical Products Corp. Williamston, MI Intended use: Vascular access port kit |
| Product code | LRS |
| Recalling firm | Centurion Medical Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 16, 2011 |
| FEI number | 1824619 |
At a glance
- None 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