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 cpap pro device's sound abatement foam.The patient has alleged malignant neoplasm of prostate, neoplasm of uncertain behavior of skin, early stage of copd and hypertension.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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