Device recall
Z-2027-2008: Cytomics FC 500 Flow Cytometry System with CXP Software Version 2.1 and 2.2 - SW…
FDA device recall · Class II · Beckman Coulter Inc
Key facts
| Recall number (Z-number) | Z-2027-2008 |
|---|---|
| Recall event | 46287 |
| Product | Cytomics FC 500 Flow Cytometry System with CXP Software Version 2.1 and 2.2 - SW Kit, CXP Analyis SW V2.2 Single User Upgrade, Automated differential cell counter; Part Number 774198; Beckman Coulter; Miami, FL 33196. |
| Product code | GKZ |
| Recalling firm | Beckman Coulter Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2011 |
| FEI number | 2050012 |
At a glance
- None Linked 510(k)s
- 10–99 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