Medscape

Class I Recall of GE Healthcare TruSignal SpO2 Sensors

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 ...
Healio

FDA identifies GE HealthCare recall of sensors for defibrillators as class I

Please provide your email address to receive an email when new articles are posted on . GE HealthCare recalled its SpO2 sensors due to a malfunction that may reduce defibrillation energy without ...
FierceBiotech

GE HealthCare lands FDA Class I recall for 81K-plus defective pulse oximetry sensors

GE HealthCare is warning healthcare providers that tens of thousands of its TruSignal pulse oximeters sold in the last few years could potentially put hospitalized patients at risk of a worsened ...