Device recall
Z-2220-2024: CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
FDA device recall · Class II · Centers For Disease Control and Prevention
Key facts
| Recall number (Z-number) | Z-2220-2024 |
|---|---|
| Recall event | 94739 |
| Product | CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11 |
| Product code | OZE |
| Recalling firm | Centers For Disease Control and Prevention |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2025 |
| 510(k) numbers | K200370 |
| FEI number | 1050190 |
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