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 previously received information alleging an issue related to a cpap device's sound abatement foam.The patient that the device was not pushing air normally.In addition, the patient reported stomach pain and a feeling of drowning in their sleep.There was no report of serious patient harm or injury.The device was returned for evaluation.Review of the error log found two error codes.However, the reported symptom was unable to be confirmed.The device passed final testing.
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