Device recall
Z-0892-2022: First SIGN SARS-CoV-2 Antigen Test
FDA device recall · Class II · WHPM Inc.
Key facts
| Recall number (Z-number) | Z-0892-2022 |
|---|---|
| Recall event | 89676 |
| Product | First SIGN SARS-CoV-2 Antigen Test |
| Product code | QKP |
| Recalling firm | WHPM Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2025 |
| FEI number | 3003102569 |
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