Quidel Corporation recalls QuickVue Dipstick Strep A Test
- Recalling company
- Quidel Corporation
- Product
- QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
- Reason
- Product has the potential for false positive results
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 6, 2026
- Reported
- May 20, 2026
- Distribution
- US Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD, MN, MO, NY, PA, SC, TN, TX, VA.
- Status
- Ongoing
- Quantity
- 12279 units
- Lot / codes
- UDI/DI 30014613201083, Lot Numbers: 225788, 228322, 233274.
- Company location
- San Diego, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2169-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2169-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.