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 sound abatement foam.The patient has alleged the device gradually blowing the air harder at high pressure and inconsistent in device pressure setting.There was no report of harm or injury.The manufacturer's investigation is ongoing.Upon completion of the investigation, a follow up report will be filed.
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