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 alleged the device was showing error service required and screen was flashing.There was no patient harm or injury reported.The device was returned to the manufacturer, and it was sent to a third-party service center for evaluation.During the evaluation in the service center, it was observed that there were visible foam particles in the device.The unit was scrapped.
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