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 a patient passed away due to the device.The manufacturer received information alleging kidney disease, asthma, liver disease, lung disease, heart issue, pulmonary embolism, copd and rectal and lung cancer.No medical intervention was specified by the patient.The device has not yet been returned to the manufacturer for evaluation.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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