ClearanceBrief
Recall Z-1668-2015 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

SIEMENS Axiom Luminos dRF Max, a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a digital flat detector, it can perform a range of applications including general R/F, angiography and pediatric examinations. The Axiom Luminos dRF is a device intended to visualize anatomical structures by converting a pattern of X-ray into a visible image.

DateMay 23, 2015 (initiated Apr 13, 2015)
StatusTerminated
ReasonStudy and all acquired images deleted when using systems with software version VE10E. Acquisitions have to be repeated. Connection with portable detectors (MAX wi-D, MAX mini) is sporadic in image recovery. Pressing undo button on the RAD subtask card or previous series button on the Image subtask card during image readout. Sporadically, during an automatic or a manual RIS update.
Root causeSoftware design
ActionA safety advisory notice, dated April 13, 2015, was sent to end users with affected devices to alert them about the issue and associated risks,and to provide instructions for avoiding potential risk. A new software version will be released to permanently resolve the issue.
Quantity133 total
DistributionNationwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K062623AXIOM LUMINOS DRF
Siemens Medical Solutions USA, Inc., Aug 22, 2007