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, the third party service center visually inspected the device and found no evidence of foam degradation.It was also determined that there was tobacco contamination and fluid in the device, the lcd screen was cracked, the upper enclosure buttons are damaged.Eval noted in ra 314658853.The device was scrapped.
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