MalfunctionGWQ
TREX
Received Jan 17, 2020 · Event occurred Nov 6, 2019
Report 9601216 · MDR key 9601216
Device
Generic name
Full-montage Standard Electroencephalograph
Product problems
- Use of Device Problem
Patient
20075 DA
- No Consequences Or Impact To Patient
- No Consequences Or Impact To Patient
Narrative
Description of Event or Problem
PATIENT FELT THAT THE A-EEG EQUIPMENT MAY HAVE BEEN FREQUENTLY BUT NOT CONSTANTLY INTERFERING WITH HIS PM-DEFIBRILLATOR DEVICE. THE A-EEG BATTERIES AND ELECTRODES WERE REMOVED AND PATIENT STATED THE PROBLEM "SEEMED" TO STOP. THERE ARE NO COMPLAINTS WHEN THE A-EEG EQUIPMENT WAS CONNECTED TO HIM IN THE LAB. THERE IS NO KNOWN HARM TO THE PATIENT.