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 patient alleged insomnia, olfactory disorders, nosebleeds, sore throat, low vision, neck pain, spinal twist, whole body spasms, thyroid enlargement, abnormal electrocardiograms, prostate enlargement, and cancer.There was no medical intervention required by the patient.The manufacturer is submitting a final report at this time.If pertinent information becomes available to the manufacturer at a later date, an addendum to this final report will be filed.
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