Diagnostica Stago
19 devices · 19 adverse event reports · 1 deaths reported · 13 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.
- STA® - Liatest® D-Di 00515FIBRINOGEN AND FIBRIN SPLIT PRODUCTS, ANTIGEN, ANTISERUM, CONTROL2 recalls0 reports
- STA Satellite® 58104SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES1 recall1 report
- STA® - Liatest® Free Protein S 6 00516TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY1 recall0 reports
- Asserachrom® HPIA 00615PLATELET FACTOR 4 RADIOIMMUNOASSAY1 recall0 reports
- STA® - Néoplastine® CI 10 00666TEST, TIME, PROTHROMBIN1 recall0 reports
- STA® - Néoplastine® CI Plus 10 00667TEST, TIME, PROTHROMBIN1 recall0 reports
- STA® - System Control N + P 00678PLASMA, COAGULATION CONTROL1 recall0 reports
- STA® - Staclot® Protein S 00746TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY1 recall0 reports
- STA® - Liquid Anti-Xa 4 00311USASSAY, HEPARIN1 recall0 reports
- STA® - Liquid Anti-Xa 8 00322USASSAY, HEPARIN1 recall0 reports
- STA® - Owren-Koller 00360General purpose reagent1 recall0 reports
- STA® - Fibrinogen 5 00674SYSTEM, FIBRINOGEN DETERMINATION1 recall0 reports
- STA® - Unicalibrator 00675PLASMA, CONTROL, NORMAL1 recall0 reports
- STA Compact Max® (with cap piercing option) 58989SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES6 reports
- STA-R Evolution® Expert Series 58978SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES1 death5 reports
- STA Compact Max® 58990SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES2 reports
- STA R Max® (with cap piercing option) 59010SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES2 reports
- STA R Max® (with cap piercing option) 59027SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES2 reports
- STA® - Cleaner Solution 00973General purpose reagent1 report