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.Per the legal department, the patient has alleged respiratory tract irritation, dizziness and/or headache, hypersensitivity, nausea/vomiting, asthma (new or worsening), inflammatory response, kidney disease/toxicity, liver disease/toxicity, and lung disease.The complaint reports that the patient has passed away (death).No other clinical information or medical intervention was 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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