Drug recall
First SIGN SARS-CoV-2 Antigen Test
FDA recall event 89676 · Class II · WHPM Inc.
Key facts
| Event ID | 89676 |
|---|---|
| Recall numbers | Z-0892-2022 |
| Recalling firm | WHPM Inc. |
| Product type | Devices |
| Products | First SIGN SARS-CoV-2 Antigen Test |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Frm became aware that a customer complaint was reported to US FDA that SARS-CoV-2 Antigen Tests were sold domestically by a pharmacy in California. These Antigen Tests have not received FDA Emergency… |
| Initiation date | Mar 4, 2022 |
| Report date | Apr 13, 2022 |
| Termination date | Feb 5, 2025 |
| City | Irwindale |
| State | CA |
| Country | United States |
| FEI number | 3003102569 |
At a glance
- 1–9 Products in this recall
- 10–99 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: