FDAJanuary 12, 2015device
Servo-I ventilator system CO2 analyzer. Part number 65 23 588.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A calibration problem was detected in a specific number of the Servo-I ventilator system CO2 analyzer models that may have been caused by the module's internal circuit board function.
What to do
FDA enforcement status: Terminated
Brands named
maquet cardiovascular us salesmaquetmaquet cardiovascular
Recall history
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