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 nose irritation, respiratory tract irritation and inflammatory response.There was no allegation of serious or permanent harm or injury.No further clinical details or medical intervention were reported.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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