Device recall
Z-1195-2014: CELLTRACKS ANALYZER II (Product Code 9555) Product Usage: The CELLTRACKS…
FDA device recall · Class II · Veridex, LLC
Key facts
| Recall number (Z-number) | Z-1195-2014 |
|---|---|
| Recall event | 67447 |
| Product | CELLTRACKS ANALYZER II (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II is a semi-automated fluorescence microscope, consisting of the analyzer, a dedicated computer with CELLTRACKS software, monitor, keyboard, mouse and uninterruptible power supply (UPS). The system also supports an… |
| Product code | NQI |
| Recalling firm | Veridex, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 6, 2017 |
| 510(k) numbers | K050145 |
| FEI number | 3004619490 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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