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All product recalls associated with Tecan US, Inc..
Total Recalls
5
Past Year
0
Class I (Serious)
0
Most Recent
Nov 2014
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Incorrect lumi firmware version installed (E.027 instead of V2.00)
Incorrect lumi firmware version installed (E.027 instead of V2.00)
Distortion (noise interference) of the liquid level capacitance can result in air aspiration instead of liquid aspiration. This might cause a false signal (air detection) with possible dispense errors resulting in erroneous results.
Double filtering of 1000 l tips. The defect could result in cross contamination of other samples due to possible dripping of sample while moving over other samples.
Tecan software has the potential to match the patient with a different patient's test results.