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 dreamstation bipap autosv device's sound abatement foam.The patient alleged nose irritation, hypersensitivity, nausea / vomiting, cancer.No further clinical details or medical intervention were reported.Due to potential litigation surrounding this case, no follow up can be performed at this time.If any additional information is received, a follow up report will be filed.
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