QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
Product has the potential for false positive results
Quick Facts at a Glance
- Recall Date
- April 6, 2026
- Hazard Level
- HIGH
- Brand
- Quidel
- Geographic Scope
- 1 states
Hazard Information
Product has the potential for false positive results
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Quidel Corporation or your healthcare provider for instructions. Notification method: Letter
Get instant alerts for Quidel recalls
Be the first to know. Free instant alerts to your inbox.
Full Description
QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.. Reason: Product has the potential for false positive results. Classification: Class II. Quantity: 12279 units. Distribution: US Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD, MN, MO, NY, PA, SC, TN, TX, VA.
Browse More Recalls
Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
Read: How to Get Refunds and ReplacementsWant to Know First?
Get instant alerts for recalls that affect you. Free forever.