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 patient alleges dizziness and/ or headache.Medical intervention was not specified.The manufacturer was made aware of this complaint through a representative of the customer.At this time, no further investigation can be requested at this time.If any additional information is received, a follow-up report will be filed.
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