Device recall
Z-1950-2013: CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage: The…
FDA device recall · Class II · Veridex, LLC
Key facts
| Recall number (Z-number) | Z-1950-2013 |
|---|---|
| Recall event | 64304 |
| Product | CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage: The CELLTRACKS AUTOPREP System is a general purpose laboratory instrument used with immunomagnetic reagents that capture and enrich target cells, and labeling reagents that differentiate cells in whole blood. Cell analyzers such… |
| Product code | NQI |
| Recalling firm | Veridex, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 11, 2015 |
| 510(k) numbers | K110406, K122821 |
| 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