The manufacturer received information regarding a dreamstation auto cpap device.The device was returned to a third-party service center.During visual inspection of the device, contamination from connector oxide on the device was found.In addition, the inspection found error code (53) and the device was scrapped.This report is being submitted for the contamination from connector oxide on the device during service.There was no allegation of serious or permanent harm or injury.No medical intervention was required for the patient.
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