MAUDE Adverse Event Report: GE OEC MEDICAL SYSTEMS 9800

Device Problem Failure to Power Up (1476)

Patient Problems No Known Impact Or Consequence To Patient (2692); No Information (3190)

Event Date 07/07/2015

Event Type  No Answer Provided  

Event Description

The customer reported that the system could not boot up.There was no patient injury or death reported.

Manufacturer Narrative

A ge service representative performed an onsite investigation.The power control board was replaced during the service call.The system was tested and found to be working as intended and put back into service.

• Brand Name: 9800
• Manufacturer (Section D): GE OEC MEDICAL SYSTEMS; 384 wright brothers dr.; salt lake city UT 84116
• Manufacturer Contact: 384 wright brothers dr.; salt lake city, UT 84116 ; 8015364952
• MDR Report Key: 4948990
• MDR Text Key: 6636447
• Report Number: 1720753-2015-03031
• Device Sequence Number: 1
• Product Code: JAA
• Combination Product (y/n): N
• PMA/PMN Number: NA
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Health Professional,User Facility,Company Representative
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 07/27/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/27/2015
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 07/07/2015
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 01/01/2000
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1