Device recall
Z-2327-2011: Material DT12210, CENTRAL LINE PROCEDURE KIT, CENTURION CENTRAL LINE PROCEDURE…
FDA device recall · Class II · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-2327-2011 |
|---|---|
| Recall event | 58346 |
| Product | Material DT12210, CENTRAL LINE PROCEDURE KIT, CENTURION CENTRAL LINE PROCEDURE KIT, REORDER DT12210, STERILE, CENTURION MEDICAL PRODUCTS CORP. WILLIAMSTON MI 48895, USA 800.248.4058 www.centurionmp.com FACILITATES LINE INSERTION DT12050 PORT ACCESS TRAY |
| 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