FDA Adverse Event Malfunction Summary report: N

DISCOVERY MR450

MDR report key: 2519750 · Received April 4, 2012

Report

Report Number
2183553-2012-00021
Event Type
Malfunction
Date Received
April 4, 2012
Date of Event
March 6, 2012
Report Date
March 6, 2012
Manufacturer
GE MEDICAL SYSTEMS, LLC
Product Code
LNH
PMA / PMN Number
K091536
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS MALFUNCTION WAS NOT REPORTED FOR A SPECIFIC SYSTEM BUT IT WAS IDENTIFIED DURING A GE HEALTHCARE (GEHC) INVESTIGATION SO DEVICE SERIAL NUMBER IS NOT APPLICABLE (N/A). INITIAL REPORTER INFO IS NOT APPLICABLE AS THIS WAS REPORTED DURING A GE HEALTHCARE (GEHC) INVESTIGATION. THIS MALFUNCTION WAS NOT REPORTED FOR A SPECIFIC SYSTEM BUT IT WAS IDENTIFIED DURING A GE HEALTHCARE (GEHC) INVESTIGATION SO DEVICE MFG DATE IS NOT APPLICABLE (N/A).

Description of Event or Problem · 1

DURING A GE HEALTHCARE INVESTIGATION OF A REPORT THAT T1 WEIGHTED CUBE IMAGES WERE FLIPPED HORIZONTALLY WHEN THESE IMAGES WERE REFORMATTED (MDR 2183353-2012-00014), IT WAS FOUND THIS COULD ALSO OCCUR IN THE DISCOVERY MR450 MR SCANNER. THE ORIENTATION MARKERS DO NOT FLIP WITH THE IMAGE. T1 WEIGHTED IMAGES ARE COMMONLY USED FOR TUMOR DETECTION OR DELINEATION IN CONJUNCTION WITH A CONTRAST AGENT. CERTAIN PATHOLOGY WOULD ONLY BE APPARENT ON THIS SEQUENCE. THIS EVENT DID NOT RESULT IN A MISDIAGNOSIS OR PT INJURY. AS THE BRAIN ANATOMY IS SYMMETRICAL A FLIP MAY NOT BE OBVIOUS TO THE CAREGIVER AND HAS A POTENTIAL OF A MISDIAGNOSIS OR MISTREATMENT. GE HEALTHCARE'S INVESTIGATION INTO THE REPORTED OCCURRENCE IS ONGOING. A FOLLOW UP REPORT WILL BE SUBMITTED WHEN THE INVESTIGATION HAS BEEN COMPLETED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DISCOVERY MR450 MAGNETIC RESONANCE DIAGNOSTIC DEVICE LNH GE MEDICAL SYSTEMS, LLC

Patients

Seq Age Sex Outcome Treatment
1