ClearanceBrief
Recall Z-0711-2018 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.

DateSep 28, 2017
StatusTerminated
ReasonThe possibility exists for the wireless foot switch to fail due to impacts by external factors, such as electrostatic discharge that exceed a certain intensity. If the foot switch fails, it will no longer be able to be used to release radiation. The hand switch provided can be used to release exposures; however, fluoroscopic examinations will not be possible.
Root causeDevice Design
ActionLetters were sent to all consignees with instructions to contact their service provider to arrange for an appointment to update the device hardware.
Quantity142
DistributionDistributed in XX states: Ak, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY, the District of Columbia, Guam, and Puerto Rico.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K010721AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM
Siemens Medical Corp., Mar 30, 2001
K021021MODULAR ANGIOGRAPHY SYSTEM AXIOM ARTIS
Siemens Medical Solutions USA, Inc., Jun 6, 2002
K052202AXIOM ARTIS - MODULAR ANGIOGRAPHIC SYSTEM
Siemens Medical Solutions USA, Inc., Mar 7, 2006