Device recall
Z-0693-03: Access 2 immunoassay side of LXi 725
FDA device recall · Class III · Beckman Coulter Inc
Key facts
| Recall number (Z-number) | Z-0693-03 |
|---|---|
| Recall event | 25601 |
| Product | Access 2 immunoassay side of LXi 725 |
| Recalling firm | Beckman Coulter Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 1, 2004 |
| 510(k) numbers | K023049 |
| FEI number | 2050012 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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