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 related to a cpap device's sound abatement foam.The patient has alleged difficulty breathing, nasal/throat irritation or soreness, sinus issue.There was no report of patient 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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