Device recall
Z-0481-2022: ImmunoPass, COVID-19 Neutralizing Antibody Test, NAB 900-60
FDA device recall · Class I · Empowered Diagnostics LLC
Key facts
| Recall number (Z-number) | Z-0481-2022 |
|---|---|
| Recall event | 89315 |
| Product | ImmunoPass , COVID-19 Neutralizing Antibody Test, NAB 900-60 |
| Product code | QKO |
| Recalling firm | Empowered Diagnostics LLC |
| Recall class | Class I |
| Status | Completed |
| FEI number | 3017977164 |
At a glance
- None 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