Medical device recalls Moderate risk

Quidel Corporation recalls QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.

Recall date
April 6, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2169-2026
FDA classification
Class II
Brand / firm
Quidel Corporation
Sold / distributed
US Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD, MN, MO, NY, PA, SC, TN, TX, VA.

Why it was recalled

Product has the potential for false positive results

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.

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