FDA Adverse Event Malfunction Summary report: N

REVOLUTION XR/D

MDR report key: 2495954 · Received March 8, 2012

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

Additional Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

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