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 voluntary medwatch (mw5149341).The manufacturer received information alleging an issue related to a philips cpap device's sound abatement foam.The patient has alleged without therapy the condition is getting worse, and the patient had undergone another sleep study.There was no report of serious or permanent patient harm or injury.No medical intervention was required by the patient.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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