A device was returned to philips 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 philips service center, the device was visually inspected and found blower foam degradation.The investigation and testing are ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.In addition, patient alleges irritation in throat and dried out and headache.
|