DIAGNOSTICA STAGO INC
STA SATELLITE · General Hospital
510(k) Clearances (2)
Substantially Equivalent
Substantially Equivalent
Recalls (10)
After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.
Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.
Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.
Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.
Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.
Potential for shorter clotting times in clotting tests which have a dilution, leading to possible overestimate of around 1%
QC values outside of the assigned ranges (prolonged Prothrombin time / decreased PT %)
Diagnostica Stago Inc. received some customer complaints regarding a misreading of Reagent 1 (substrate) barcode on STA analyzers.
Following a single customer complaint that incorrect INR values were occasionally printed for PT tests, even though the primary units (seconds) were correct, the firm investigated and confirmed the potential for printing incorrect secondary units when using an external printer and the customer printout mode on the STA Satellite.
Factor VIII quality control results are being recovered below the assigned ranges for STA System Control N+P.
FDA Classification (66)
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