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 has alleged to have headaches and seizures.A neurologist did do testing and found no cause for the headaches.The patient believes it is a coincidence since this recall came out.During that test, he did have to wear a device on his head for a week to follow head activity.Headaches began 2-3 years ago.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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