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 alleged of having bronchitis, chronic sinusitis, lung injury/ damage, respiratory irritation, congestion, sore throat, cough, heart failure, acute respiratory failure, asthma from a dreamstation auto cpap device.Medical intervention was not specified.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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