The manufacturer was contacted 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 an issue related to a cpap device's sound abatement foam.The patient has alleged pain above the eye after using the device and states the pain goes away upon waking.The patient stated this has occurred for approximately one year with use of the device.There was no report of serious patient harm or injury.There was no medical intervention was required by the patient.The device was returned and evaluated by the manufacturer.The internal part of the device was inspected visually.The device's downloaded logs were reviewed by the manufacturer and 2 error was found.The manufacturer concludes that no visible foam degradation was found and could not confirm customer's complaint.No problem found the device was scrapped.
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