Device recall
Z-2305-2011: Material CVI2970, UNIVERSAL INSERTION / PROTECTION KIT, CENTURION UNIVERSAL…
FDA device recall · Class II · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-2305-2011 |
|---|---|
| Recall event | 58346 |
| Product | Material CVI2970, UNIVERSAL INSERTION / PROTECTION KIT, CENTURION UNIVERSAL INSERTION/PROTECTION KIT, REORDER CVI2970, STERILE, LATEX FREE, CENTURION MEDICAL PRODUCTS CORP. WILLIAMSTON MI 48895, USA 800.248.4058 www.centurionmp.com FACILITATES LINE PLACEMENT |
| 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