Quidel recalls QuickVue Dipstick Strep A Test (50T) with potential for false positives. Affected units include specific lot numbers and reference codes. Consumers should check their product details.
Product has the potential for false positive results
Quidel is recalling its QuickVue Dipstick Strep A Test (50 tests) due to a potential for false positive results. This could lead to incorrect diagnoses of strep throat, causing unnecessary anxiety or treatment. The recall affects specific lot numbers and reference codes.
The test may show a positive result for strep throat when there is no infection, leading to false diagnoses. This can cause unnecessary stress and inappropriate antibiotic use. The false positive risk is specific to the recalled product batches.
People who purchased the QuickVue Dipstick Strep A Test (50 tests) with reference code 20108 and specific lot numbers (225788, 228322, : 233274) are affected. Those using the test for strep throat diagnosis are most at risk of incorrect results.
Check the product's reference code (20108) and lot numbers (225788, 228322, 233274) on the packaging. The test is for strep A detection and comes in a 50-test package.
Look for the reference code 20108 and lot numbers 225788, 228322, or 233274 on the packaging.
The recall is due to a potential for false positive results, which could lead to incorrect strep throat diagnoses.
Check the reference code and lot numbers on the packaging. If it matches the recalled items, contact Quidel for further instructions.
The test is safe to use, but the recall is for potential false positives, not safety hazards.
We’ve drafted a message you can send Quidel to request your refund or repair — edit it as you like.
Subject: Recall Z-2169-2026 — Quidel Quidel Hello, I own a Quidel that is covered by recall Z-2169-2026 from Quidel. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
