Device recall
Z-2223-2011: V-CATH Insertion Kits, Sterile; Product Code Number: 301-00; Manufactured by…
FDA device recall · Class II · Neo Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2223-2011 |
|---|---|
| Recall event | 58514 |
| Product | V-CATH Insertion Kits, Sterile; Product Code Number: 301-00; Manufactured by Centurion Medical Products for Neo Medical; 42514 Albrae Street, Fremont, CA 94538 |
| Product code | LRS |
| Recalling firm | Neo Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 22, 2011 |
| FEI number | 2925153 |
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