Drug recall
INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
FDA recall event 93626 · Class II · PHASE SCIENTIFIC INTERNATIONAL LIMITED
Key facts
| Event ID | 93626 |
|---|---|
| Recall numbers | Z-0738-2024 |
| Recalling firm | PHASE SCIENTIFIC INTERNATIONAL LIMITED |
| Product type | Devices |
| Products | INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | COVID-19 rapid antigen at home tests were released with an incorrect expiration date of 05 April 2024 when the correct expiration should be 21 February 2024. Expired tests could produce invalid or… |
| Initiation date | Oct 25, 2023 |
| Report date | Jan 24, 2024 |
| City | Sha Tin |
| Country | Hong Kong SAR |
| FEI number | 3017887566 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: