Device recall
Z-0263-05: Immulite 2500 Automated Immunoassay Analyzer, Human chorionic gonadotrpin (HCG)…
FDA device recall · Class II · DPC Cirrus
Key facts
| Recall number (Z-number) | Z-0263-05 |
|---|---|
| Recall event | 30394 |
| Product | Immulite 2500 Automated Immunoassay Analyzer, Human chorionic gonadotrpin (HCG) test system. |
| Product code | DHA |
| Recalling firm | DPC Cirrus |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 18, 2005 |
| 510(k) numbers | K033234 |
| FEI number | 1000122204 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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