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 cpap device's sound abatement foam.The patient has also reported having stroke.The relationship between the device and the stroke is currently unclear.The device was returned and manufacturer could not confirm customer complaint and there was no problem found during device evaluation.Medical intervention was not specified.
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