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 headache, sore throat and extreme dry, irritated eyes.There was no report of serious or permanent patient harm or injury.The device was returned to a third-party service center for evaluation.There was no evidence of visible foam particles.The customer's complaint could not be confirmed.In addition, the device has been scrapped.
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