--- title: "Quidel Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Quidel Corporation recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/quidel-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Quidel Corporation recall records **6** reported ongoing 6 records in this archive. Latest source date Apr 6, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Apr 6, 2026 FDA device enforcement ### [QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.](https://isitonrecall.com/recall/fda-device-z-2169-2026-quickvue-dipstick-strep-a-test-50t-ref-20108-antigens-all-groups-streptococcus-spp/) Product has the potential for false positive results Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD, MN, MO, NY, PA, SC, TN, TX, VA. [Official source for QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2169-2026%22) Jun 17, 2025 FDA device enforcement ### [QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC](https://isitonrecall.com/recall/fda-device-z-2545-2025-quickvue-dipstick-strep-a-test-50t-ref-20108-25t-ref-20125-50t-scn-ref-20108sc/) Dipstick strep A test has potential for false positive results. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of MA, NJ, MD, NC, SC, FL, TN, MS, MN, IL, MO, KS, LA, TX, CO, ID, CA, AK, NY, PA and the countries of Canada, Italy, Denmar... [Official source for QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2545-2025%22) Mar 5, 2024 FDA device enforcement ### [QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests](https://isitonrecall.com/recall/fda-device-z-1636-2024-quidel-inflammadry-mmp-9-test-ref-prs-id-20-u-20-tests/) There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test results, the positivite test line may not be visible/ hidden under the cassett... Class II Reported ongoing Distribution: US: AK AL AR AZ CA CO CT DC FL GA HI IA ID IL IN KS KY LA MA MD MI MN MO MT NC ND NE NH NJ NV NY OH OK OR PA SC SD TN TX UT VA WA WI WV OUS: United Arab Emirates, Belgium, Canad... [Official source for QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1636-2024%22) Mar 5, 2024 FDA device enforcement ### [QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests](https://isitonrecall.com/recall/fda-device-z-1637-2024-quidel-inflammadry-mmp-9-test-ref-prs-id-20-20-tests/) There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test results, the positivite test line may not be visible/ hidden under the cassett... Class II Reported ongoing Distribution: US: AK AL AR AZ CA CO CT DC FL GA HI IA ID IL IN KS KY LA MA MD MI MN MO MT NC ND NE NH NJ NV NY OH OK OR PA SC SD TN TX UT VA WA WI WV OUS: United Arab Emirates, Belgium, Canad... [Official source for QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1637-2024%22) Jan 3, 2024 FDA device enforcement ### [The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design that is used with Sofia 2 to detect nucleocapsid protein from influenza A, influenz...](https://isitonrecall.com/recall/fda-device-z-1086-2024-the-sofia-2-flu-sars-antigen-fia-employs-immunofluorescence-technology-in-a-sandwich-design-that-is/) One lot of the Sofia 2 Flu + SARS Antigen FIA (Lot 709083) was labelled with incorrect expiration dates. The kits contain pouched cassettes labeled with an expiration date of May 31, 2025, however the correct expiration date for the pouches is September 12,... Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, TN, IL, LA, NY, IN. [Official source for The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design tha...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1086-2024%22) Feb 1, 2023 FDA device enforcement ### [MicroVue C1-Inhibitor Plus EIA for measuring the amount of functional C1-lnhibitor protein in human plasma or serum, Catalog Number A037, Containing Coated Strips, REF: 4634, wi...](https://isitonrecall.com/recall/fda-device-z-1308-2023-microvue-c1-inhibitor-plus-eia-for-measuring-the-amount-of-functional-c1-lnhibitor-protein-in-human/) Kits with affected microtiter plates have the potential to produce low OD values, causing the run to fail, per the Validation requirements of the Package Insert. Class II Reported ongoing Distribution: not yet available [Official source for MicroVue C1-Inhibitor Plus EIA for measuring the amount of functional C1-lnhibitor protein in hum...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1308-2023%22) ## Reasons in these listed records - Product has the potential for false positive results - Dipstick strep A test has potential for false positive results. - There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test results, the positivite test line may not be visible/ hidden under the cassette of the test device... - One lot of the Sofia 2 Flu + SARS Antigen FIA (Lot 709083) was labelled with incorrect expiration dates. The kits contain pouched cassettes labeled with an expiration date of May 31, 2025, however the correct expiration date for the pouches is September 12, 2024. The kits are ... These examples come from this result page and are not a ranking of every recall reason. ## Checking Quidel Corporation ### Is there a recall on quidel corporation right now? This archive contains 6 records, including 6 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Quidel Corporation](https://isitonrecall.com/check/?q=Quidel%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)