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QuickVue Dipstick Strep A Test
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MEDICAL DEVICE RECALLMODERATE

QuickVue Dipstick Strep A Test

Quidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.

What to do

Stop using this test kit immediately. Contact Quidel Corporation for replacement or refund instructions. Do not rely on results from affected units for clinical decision-making.

Posted
Updated
Recall No.
Z-2169-2026
Agency
Firm
Quidel Corporation
Recall ID
98709
Status
ONGOING

Why it was recalled

Product has the potential for false positive results

How to identify it

UPC 30014613201083

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

Where it was sold

Distributed in US.

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Editorial summary by Recall Canary · last updated 2026-05-13 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification