A device was returned to a third-party service center in reference to the voluntary field safety notice / recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.There was corrosion present in device and corrosion in connector.In addition, the inspection found other contamination of connector oxide was found inside the device.There is no allegation of serious or permanent harm or injury.During the evaluation of the device, the third-party service visually inspected the device and found corrosion in device.The device was scrapped.
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