Drug recall
QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
FDA recall event 98709 · Class II · Quidel Corporation
Key facts
| Event ID | 98709 |
|---|---|
| Recall numbers | Z-2169-2026 |
| Recalling firm | Quidel Corporation |
| Product type | Devices |
| Products | QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product has the potential for false positive results |
| Initiation date | Apr 6, 2026 |
| Report date | May 20, 2026 |
| City | San Diego |
| State | CA |
| Country | United States |
| FEI number | 2024674 |
At a glance
- 1–9 Products in this recall
- 1–9 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: