FDA Class II · Medical device · May 20, 2026
QuickVue Dipstick Strep A Test recall — Quidel Corporation
Product has the potential for false positive results
Official ID Z-2169-2026 · Official record ↗
Quidel recalls
Recall found. Quidel is named in FDA Class II recall Z-2169-2026 covering QuickVue Dipstick Strep A Test. Hazard: Product has the potential for false positive results Identifying details: UDI/DI 30014613201083, Lot Numbers: 225788, 228322, 233274.. Status: Ongoing.
Models with recalls
All Quidel recalls
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.