Class II

Medical Device Recall: QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC

Quidel Corporation · June 17, 2025

Reason for Recall

Dipstick strep A test has potential for false positive results.

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, Denmark, Norway, Sweden, Finland, Thailand, Israel, Slovenia, Turkey.

States Affected

NATIONWIDE

Quantity Affected

22470

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2545-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.