Device recall
Z-1084-2011: Centurion Medical Products Central line procedure kit DT12210, Sterile
FDA device recall · Class II · Centurion Medical Products
Key facts
| Recall number (Z-number) | Z-1084-2011 |
|---|---|
| Recall event | 56391 |
| Product | Centurion Medical Products Central line procedure kit DT12210, Sterile |
| Product code | LRS |
| Recalling firm | Centurion Medical Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 9, 2011 |
| FEI number | 1824619 |
At a glance
- None Linked 510(k)s
- 10–99 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