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 difficulty breathing/short of breath.The patient also alleged device not functioning/device will not turn on.There is no allegation of serious or permanent harm or injury.No medical intervention was specified by the patient.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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