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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

Quidel Corporation is recalling QuickVue Dipstick Strep A Test, 50T (REF 20108) due to the potential for false positive results. Affected units may incorrectly indicate the presence of Group A Streptococcus when the infection is not present. Stop using the product and contact Quidel Corporation for instructions on replacement or refund.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

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

UPC
30014613201083
Recall #
Z-2169-2026

Where it was sold

Distributed nationwide.

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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