GE Healthcare Finland Oy: TruSignal Wrap Sensor, REF TS-W-D; Oximeter
Recall reason: There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.. Recalled by GE Healthcare Finland Oy. Distribution: Worldwide. Classification (Class I — serious health hazard). Affected lots/dates: GTIN 00840682103121. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.
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