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 blocked tear ducts.Medical intervention was not specified.The patient required admitted to hospital for 2 surgical procedures, right dcr and left dcr.Now his doctor stopped him using the philips device.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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