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.The manufacturer received information alleging device burning rubber like smell and very noise.There was no report of patient harm or injury.The device was returned to a third-party service center for investigation.During the evaluation of the device, the third-party service center visually inspected the device and found no evidence of foam.Degradation.The customer's complaint was not confirmed.No other secondary finding available.The device was scrapped.At this time, no further investigation can be performed.If any additional information is received, a follow up report will be filed.
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