Device recall
Z-2936-2020: Parvovirus B19 IgG EIA kit Part No. V519IGUS
FDA device recall · Class II · Diasorin Inc.
Key facts
| Recall number (Z-number) | Z-2936-2020 |
|---|---|
| Recall event | 86152 |
| Product | Parvovirus B19 IgG EIA kit Part No. V519IGUS |
| Product code | MYL |
| Recalling firm | Diasorin Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P970054 |
| FEI number | 2182595 |
At a glance
- None 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