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 odor coming from device.The patient alleges coughing, wheezing, sinus congestion, clear discharge of sputum, headaches, difficulty breathing.There is no allegation of serious or permanent harm or injury.The patient required blood work, allergy testing, lung parameters.The patient reported no medication was order, but was told to get exercise, take allergy medications if necessary, and get fresh air.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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