Device recall
Z-0738-2024: INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
FDA device recall · Class II · PHASE SCIENTIFIC INTERNATIONAL LIMITED
Key facts
| Recall number (Z-number) | Z-0738-2024 |
|---|---|
| Recall event | 93626 |
| Product | INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040 |
| Product code | QMN |
| Recalling firm | PHASE SCIENTIFIC INTERNATIONAL LIMITED |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3017887566 |
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