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 nasal/throat irritation, runny eyes and sneezing.There is no allegation of serious or permanent harm or injury.No medical intervention was required by the patient.The device was returned and evaluated by the manufacturer.The internal part of the device was inspected visually.The device's downloaded logs were reviewed by the manufacturer and 0 error was found.The manufacturer concludes that there was no evidence of visible foam degradation.
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