DISCOVERY MR450
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
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).
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 |