Device recall
Z-0116-2007: Venoscope Neonatal Transilluminator, Model NT01
FDA device recall · Class II · Venoscope LLC
Key facts
| Recall number (Z-number) | Z-0116-2007 |
|---|---|
| Recall event | 36548 |
| Product | Venoscope Neonatal Transilluminator, Model NT01 |
| Product code | HJN |
| Recalling firm | Venoscope LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 21, 2007 |
| 510(k) numbers | K951422 |
| FEI number | 1000306918 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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