Device recall
Z-2357-2011: Material ECVC1020, TRIPLE LUMEN BUNDLE KIT W/CATHETER, CENTURION TRIPLE LUMEN…
FDA device recall · Class II · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-2357-2011 |
|---|---|
| Recall event | 58346 |
| Product | Material ECVC1020, TRIPLE LUMEN BUNDLE KIT W/CATHETER, CENTURION TRIPLE LUMEN BUNDLE KIT WITH CATHETER, REORDER ECVC1020, LATEX FREE, STERILE, CENTURION MEDICAL PRODUCTS CORP. HOWELL MI 48843 USA 800.248.4058 www.centurionmp.com FACILITATES LINE INSERTION |
| Product code | LRS |
| Recalling firm | Centurion Medical Products Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 13, 2011 |
| FEI number | 3008403546 |
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