Device recall
Z-2053-2009: Integra NeuroSciences Ventrix Ventricular Tunneling Pressure Monitoring Kit…
FDA device recall · Class II · Integra Neuro Sciences
Key facts
| Recall number (Z-number) | Z-2053-2009 |
|---|---|
| Recall event | 51674 |
| Product | Integra NeuroSciences Ventrix Ventricular Tunneling Pressure Monitoring Kit NL950-V and Integra NeuroSciences Ventrix Ventricular Tunneling Pressure Monitoring Kit with Ventricular Drainage System NL950-VC. This intracranial pressure (ICP) catheter is indicated for use on patients that require… |
| Product code | JXG |
| Recalling firm | Integra Neuro Sciences |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 19, 2012 |
| 510(k) numbers | K904883 |
| FEI number | 2023988 |
At a glance
- 1–9 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