Quidel Corporation
15 devices · 12,105 adverse event reports · 2 deaths reported · 8 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- QuickVue 20402Coronavirus antigen detection test system.4,225 reports
- 3,695 reports
- Sofia 20377COVID-19 Multi-Analyte Antigen Device1 recall3,284 reports
- QuickVue 20387Coronavirus antigen detection test system.686 reports
- QuickVue 20398Coronavirus antigen detection test system.210 reports
- QuickVue 20108ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP.2 recalls0 reports
- Sofia 20274ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP.1 recall2 reports
- QuickVue In-Line 00345ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP.1 recall0 reports
- QuickVue 20125ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP.1 recall0 reports
- MicroVue C1-InhibitorCOMPLEMENT C1 INHIBITOR (INACTIVATOR), ANTIGEN, ANTISERUM, CONTROL1 recall0 reports
- InflammaDry RPS-ID-20MMP-9 test system1 recall0 reports
- InflammaDry RPS-ID-20-UANTIGENS, CF (INCLUDING CF CONTROL), ADENOVIRUS 1-331 recall0 reports
- QuickVue 20183ANTIGENS, CF (INCLUDING CF CONTROL), INFLUENZA VIRUS A, B, C1 death1 report
- Sofia 20218ANTIGENS, CF (INCLUDING CF CONTROL), INFLUENZA VIRUS A, B, C1 death1 report
- Sofia 20260ANTIGEN, CF (INCLUDING CF CONTROLS), RESPIRATORY SYNCYTIAL VIRUS1 report