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 reporter has alleged the patient already suffered a stroke and has major heart issues.The relationship between the device and the adverse events are currently unclear.The manufacture's investigation is ongoing.A follow up report will be submitted when the manufacture's investigation is complete.
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