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 was made aware of this complaint through a representative of the customer and alleging of eye irritation, nose irritation, sinus infection, slight elevation in kidney bun level.There was medical intervention required need to sinuplasty surgery.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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