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 from the patient alleging that the patient has swollen lymphoid causing to choke, dry cough, coughing up phlegm and trouble eating and drinking.There is no allegation of serious or permanent harm or injury.No medical intervention was required by the patient.Despite of multiple attempts the device has not yet returned to the manufacturer for evaluation.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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