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 an issue related to a dreamstation auto device's sound abatement foam.The patient has alleged the patient has alleged that his device has caused liver issues and dizziness over the years since he has used it.There was no report of serious or permanent harm or injury.Device has not been returned to the manufacture for evaluation.There was only one attempt made and it was not the correct number and there is no email address listed to reach out to the customer.If any additional information is received, a follow up report will be filed.
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