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AVEA VENTILATOR Adverse Event — Malfunction (MDR 2021710-2020-11776)

AVEA VENTILATOR Adverse Event — Malfunction (MDR 2021710-2020-11776) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AVEA VENTILATOR; Generic name: VENTILATOR, CONTINUOUS, FACILITY USE; Manufacturer: VYAIRE MEDICAL.

DeviceAVEA VENTILATOR
Generic nameVENTILATOR, CONTINUOUS, FACILITY USE
ManufacturerVYAIRE MEDICAL
Report number2021710-2020-11776
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceHEALTH PROFESSIONAL, USER FACI
NarrativeVYAIRE FILE IDENTIFICATION: (B)(4). AT THIS TIME, THE SUSPECT DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. THEREFORE, ROOT CAUSE HAS NOT BEEN DETERMINED YET.
SourceopenFDA MAUDE (device adverse events)

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