The manufacturer received a voluntary medwatch (mw5106261) 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 a "decline in my health." the patient reported allegations of fatigue, confusion, memory loss, difficulty with concentration, word recall, and sequencing, lack of motivation and depression.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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