Device recall
Z-0902-06: Unicel DxC 600/800 SYNCHRON Clinical Systems; Operating Software Version 1.0 and…
FDA device recall · Class III · Beckman Coulter Inc
Key facts
| Recall number (Z-number) | Z-0902-06 |
|---|---|
| Recall event | 35077 |
| Product | Unicel DxC 600/800 SYNCHRON Clinical Systems; Operating Software Version 1.0 and 1.2; Part Number: A20463 and A27331 |
| Product code | JJE |
| Recalling firm | Beckman Coulter Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 19, 2012 |
| 510(k) numbers | K042291 |
| 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