Device recall
Z-0901-06: SYNCHRON LX i 725 Clinical Systems; Operating Software Version 4.5; Part Number…
FDA device recall · Class III · Beckman Coulter Inc
Key facts
| Recall number (Z-number) | Z-0901-06 |
|---|---|
| Recall event | 35077 |
| Product | SYNCHRON LX i 725 Clinical Systems; Operating Software Version 4.5; Part Number: A23724 |
| Product code | JJE |
| Recalling firm | Beckman Coulter Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 19, 2012 |
| 510(k) numbers | K023049 |
| 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