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 having one eye and experiencing worse eye problems, shortness of breath, vision impairment, loss of balance, nausea, new moles on belly, headaches, dry mouth, sinus problems, congestion, throat and nasal irritation and soreness, feeling tired all the time.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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