REVOLUTION XR/D
Report
- Report Number
- 2126677-2012-00031
- Event Type
- Malfunction
- Date Received
- March 8, 2012
- Date of Event
- February 28, 2012
- Report Date
- February 28, 2012
- Manufacturer
- GE MEDICAL SYSTEMS, LLC
- Product Code
- JAA
- PMA / PMN Number
- K012389
- Removal / Correction Number
- 2126677-10/5/11-002-C
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
Narratives
THIS MALFUNCTION WAS DETERMINED TO BE REPORTABLE AS THIS SAME MALFUNCTION HAS PREVIOUSLY CONTRIBUTED TO A SERIOUS INJURY WITHIN THE LAST TWO YEARS. REFERENCE MDR 2126677-2010-00010. INITIAL REPORTER NAME AND OCCUPATION WAS NOT PROVIDED. GE HEALTHCARE'S INVESTIGATION CONCLUDED THAT THE MECHANISM WHICH APPLIES FRICTION TO THE REVOLUTION XR/D PT BARRIER PIVOTING ARM WEARS RAPIDLY ALLOWING THE ARM TO SWING FREELY WHEN THE LOCK IS NOT APPLIED. THE RESULT IS THAT THE PIVOTING ARM MAY BE STORED IN AN UPRIGHT POSITION WHICH WILL BE UNSTABLE DUE TO A LACK OF RESIDUAL FRICTION. GE HEALTHCARE WILL MODIFY THE ROTATING ARMS TO RESTORE THE RESIDUAL FRICTION SO THAT THE ARM WILL RETAIN POSITION (RATHER THAN SWING FREELY) WHILE THE LOCKING LEVERS ARE DISENGAGED. THE PRODUCT LABELING WILL ALSO BE UPDATED TO IMPROVE AWARENESS AND IDENTIFY THE HAZARD RELATIVE TO PROPER STORAGE. THE ACTION HAS BEEN REPORTED TO FDA PER 21 CFR PART 806 ON 1005/2011. REFERENCE CORRECTIONS AND REMOVALS REPORT NUMBER 2126677-20/5/11-002-C.
IT WAS REPORTED THAT A PT BARRIER ROTATIONAL HANDLE LOCK WAS BROKEN IN A MANNER THAT PREVENTED IT FROM LOCKING INTO POSITION. NO INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | REVOLUTION XR/D | STATIONARY X-RAY SYSTEM | JAA | GE MEDICAL SYSTEMS, LLC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |