Device recall
Z-2387-2008: UniCel Dxl 800 Access Immunoassay System and UniCel DxC 880i Synchron Access…
FDA device recall · Class II · Beckman Coulter Inc
Key facts
| Recall number (Z-number) | Z-2387-2008 |
|---|---|
| Recall event | 48186 |
| Product | UniCel Dxl 800 Access Immunoassay System and UniCel DxC 880i Synchron Access Clinical System |
| Product code | JJE |
| Recalling firm | Beckman Coulter Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 29, 2011 |
| 510(k) numbers | K023764 |
| FEI number | 2050012 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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