ClearanceBrief
Recall Z-0016-2014 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

Siemens RAD Fluoro Uro Systems - Luminos dRF, Ysio and Uroskop Omnia with software versions VB10D, VB10F, VB10C and VB10E. Fluroscopic X-Ray Systems

DateNov 1, 2013 (initiated May 6, 2013)
StatusTerminated
ReasonSiemens has discovered through product monitoring a potential malfunction when using system operating with software versions VB10D, VB10F, VB10C and VB10. During a RAD examination the possibility exists that radiation may continue longer than expected and may result in unnecessary dose applied during an acquisition. Additionally, it is not possible for the user to stop the radiation manually; ho
Root causeSoftware design
ActionSiemens initiated this correction on May 6, 2013 by sending Update InstructionXP005/13/S. Firm subsequently issued a letter on June 3, 2013 to all accounts. 1. Siemens Field Modification of the Luminos dRF, Ysio & Uroskop Omina running software versions VB10D, VB10F, VB10C and VB10E, which improves the signal transmission for the automatic exposure control, is available as of May 2013, and systems will be updated within one year. 2. The revised software fix for models Luminos dRF, Ysio & Uroskop Omina running software versions VB10D, VB10F, VB10C and VB10E, will be provided to all identified
Quantity23
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
K081722YSIO
Siemens Medical Solutions USA, Inc., Aug 22, 2008
K101491UROSKOP OMNIA
Siemens Medical Solutions USA, Inc., Jun 30, 2010