Device recall
Z-1044-2022: Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit; COVID 19 Test
FDA device recall · Class I · Woodside Acquisitions Inc.
Key facts
| Recall number (Z-number) | Z-1044-2022 |
|---|---|
| Recall event | 89995 |
| Product | Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit; COVID 19 Test |
| Product code | QKP |
| Recalling firm | Woodside Acquisitions Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 3022253625 |
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