The manufacturer received a voluntary medwatch mw5118721 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 pneumonia, interstitial lung disease, aspiration and death.Medical intervention was not specified.The patient required a ct scan and was hospitalized with extreme shortness of breath and passed away.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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