GE HealthCare is recalling 7559 TruSignal arterial oxygen saturation (SpO2) sensors because of problems that may reduce defibrillation energy, expose patients to unintended voltage, or give inaccurate ...

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The recall began earlier this year after GE HealthCare learned that some of its TruSignal SpO2 sensors may be at risk of malfunctioning, which the FDA has linked to flaws in the design of the devices.