Device recall
Z-1102-2007: Cell Search Circulating Tumor Cell Kit (Epithelial) Veridex LLC, a Johnson &…
FDA device recall · Class III · Veridex, LLC
Key facts
| Recall number (Z-number) | Z-1102-2007 |
|---|---|
| Recall event | 38206 |
| Product | Cell Search Circulating Tumor Cell Kit (Epithelial) Veridex LLC, a Johnson & Johnson Company IVD Veridex, LLC 33 Technology Drive Warren, NJ 07059 USA 1-877-VERIDEX USA |
| Product code | NQI |
| Recalling firm | Veridex, LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 6, 2007 |
| 510(k) numbers | K050245, K052191, K062013 |
| FEI number | 3004582358 |
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