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PHILIPS V60 VENTILATOR Adverse Event — Death (MDR 10005755)

PHILIPS V60 VENTILATOR Adverse Event — Death (MDR 10005755) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PHILIPS V60 VENTILATOR; Generic name: V60 VENTILATOR; Manufacturer: PHILIPS HEALTHCARE RESPIRONICS.

DevicePHILIPS V60 VENTILATOR
Generic nameV60 VENTILATOR
ManufacturerPHILIPS HEALTHCARE RESPIRONICS
Report number10005755
Event typeDeath
Product problemN
Date received2020-04-23
NarrativeBIPAP VENTILATOR (V60) USED AT INTUBATION OF COVID POSITIVE PT. AFTER INTUBATION AND HOOKED UP TO VENTILATOR, PT BECAME BRADYCARDIC AND HAD LOW OXYGEN SATURATION. MACHINE NOTED TO BE FUNCTIONING. CONCERN FOR RETURN VOLUME ON SCREEN WAS NOT CORRECT. DEVICE RETURNED TO MFR. PER MAINTENANCE REPORTS FROM PHILLIPS ON THE VENTILATOR INVOLVED IN THE EVENT, THE UNIT HAD PREVENTATIVE MAINTENANCE COMPLETED
SourceopenFDA MAUDE (device adverse events)

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