Device recall
Z-0572-05: Varcella Zoster ELISA Kit for the detection of IgG antibodies to varicella…
FDA device recall · Class II · Diasorin Inc.
Key facts
| Recall number (Z-number) | Z-0572-05 |
|---|---|
| Recall event | 30891 |
| Product | Varcella Zoster ELISA Kit for the detection of IgG antibodies to varicella zoster virus in human serum, Catalog No.: 4620. DiaSorin Stillwater, Minnesota 55082-0285 |
| Product code | LFY |
| Recalling firm | Diasorin Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 22, 2006 |
| 510(k) numbers | K900688 |
| FEI number | 2182595 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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