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.During the evaluation of the device at the third party service center, the device was visually inspected/scrapped and found no evidence of foam degradation.During the evaluation, corrosion to the power connector and metallic surfaces was confirmed and the device would not power on.
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