Device recall
Z-2253-2009: VEST 6.6 or earlier software for use with Neuro Kinetics products. The device is…
FDA device recall · Class II · Neuro Kinetics
Key facts
| Recall number (Z-number) | Z-2253-2009 |
|---|---|
| Recall event | 52961 |
| Product | VEST 6.6 or earlier software for use with Neuro Kinetics products. The device is used for vestibular testing. |
| Product code | LXV |
| Recalling firm | Neuro Kinetics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2010 |
| 510(k) numbers | K083603 |
| FEI number | 2519945 |
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