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/corrected and found evidence of foam degradation.During the evaluation, foam particles were visible.In addition to the above findings, top enclosure ambient sensor light cracks, ui panel screen scratch, and bottom enclosure scratch.All parts were replaced.
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