ClearanceBrief
Recall Z-0884-2013 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Philips Healthcare Inc.

Philips DigitalDiagnost X-Ray System with Eleva Software 2.1.3 Model numbers 712020, 712022, and 712082 Product Usage: Digital radiographic system

DateFeb 26, 2013 (initiated Oct 25, 2012)
StatusTerminated
ReasonWhen the operator for a wall stand view selects an "image rotation" different from default, or such image rotation is preset in the examination database, then the resulting image may be rotated in the wrong direction. When the operator manually rotates the image back, electronic side markers (if programmed) are rotated also and as a result may be placed in a wrong position inside the image.
Root causeSoftware design
ActionPhilips Medical Systems issued on October 25, 2012 an Urgent Field Safety Notice for the Digital Diagnost System informing consignees of the software upgrade. The UFSN described the problem, the hazard involved, the action to be taken by the consumer/user and the action planned by Philips. For questions contact your local Philips representative: Technical Support Line 1-800-722-9377.
Quantity551
DistributionWorldwide Distribution - USA Nationwide and the Foreign countries of: Austria, Canada, Belgium, China,Denmark, France, germany, Italy, Netherlands,New Zealand, Norway, Philippines, Portugual, SOuth Korea, Spain, Switzerland, Thailand, and UK.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K982795PHILIPS BUCKY VISION
Philips Medical Systems, Inc., Nov 24, 1998