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 alleges that he/she is having headache at night and chest pain.The patient said that he/she was in the emergency room due to wrong with the heart.The patient was examined, but was sent home and still gets the same symptoms occasionally.There is no allegation of serious or permanent harm or injury.No medical intervention was required by the patient.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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