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 difficulty breathing/short of breath and device does not always turn on.The device will not stay closed and the patient has to keep something on the device to keep it closed.There was no report of serious or permanent harm or injury.The device was returned and manufacturer confirmed the complaint.Device was found to be scrapped due to extreme dirt.
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