The manufacturer was contacted in reference to the voluntary field safety notice/recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.The manufacturer received information alleging his device auto trial mode for 15 months and now shut off.Patient also alleging throat irritation and cough.There was no report of serious or permanent harm or injury.At this time, no further investigation can be performed.If any additional information is received, a follow up report will be filed.
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