{"url_path":"/fda/device/recalls/Z-2169-2026","section_key":"summary","section_title":"DEVICE Recall: Quidel Corporation — QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-06","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2169-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Quidel Corporation"},"word_count":83,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2169-2026\n\n**Recalling firm:** Quidel Corporation\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-06\n**Report date:** 2026-05-20\n\n## Product\nQuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.\n\n## Reason\nProduct has the potential for false positive results\n\n## Affected lots\nUDI/DI 30014613201083, Lot Numbers:  225788, 228322, 233274.\n\n## Distribution\nUS Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD, MN, MO, NY, PA, SC, TN, TX, VA."}