The manufacturer received a voluntary medwatch (mw5118966) in reference to the field safety notice/recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.The patient alleges chest pain, respiratory infection, headaches, and irregular heartbeat/psv.Medical intervention was not specified.The manufacturer believes they will be unable to gather additional information.The manufacturer is submitting a final report at this time.If pertinent information becomes available to the manufacturer at a later date, an addendum to this final report will be filed.
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