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 respiratory tract irritation, new or worsening asthma and reduced cardiopulmonary reserve.There is no allegation of serious or permanent harm or injury.No medical intervention was specified as required by the patient.The manufacturer's investigation is ongoing.A supplemental follow-up report will be submitted when the manufacturer's investigation is complete.
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