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 manufacturer received information alleging visualization of particles in the air path.Patient states they did not notice particles in the device.The patient reported using an ozone based disinfection device.There was no allegation of serious or permanent harm or injury.No medical intervention was required by the patient.No other information has been received however if additional information is received a supplemental/follow up will be sent.
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