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 increased of sleep apnea and device is noisy.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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