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 dizziness, headache, inflammatory response, kidney disease/toxicity, cancer, and large cell b lymphoma.Medical intervention was not specified.The manufacturer was made aware of this complaint through a representative of the customer.No patient information was provided.No additional information can be requested at this time.The manufacturer believes they will be unable to gather additional information.The manufacturer is submitting a final report at this time.If pertinent information becomes available to the manufacturer at a later date, an addendum to this final report will be filed.
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