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GE Healthcare Finland Oy recalls TruSignal Wrap Sensor, REF TS-W-D; Oximeter
Recalled July 12, 2023 · FDA recall Z-2029-2023 · GE Healthcare Finland Oy
Hazard
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. · FDA Class I
Units
5039 units
Sold at
Worldwide
Description
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
Product
TruSignal Wrap Sensor, REF TS-W-D; Oximeter
Manufacturer(s)
GE Healthcare Finland Oy
Made in
Finland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →