Siemens Medical Solutions USA, Inc Axiom Artis X-Ray System using software version VB11D or VB20B Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Axiom Artis X-Ray System using software version VB11D or VB20B
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
model numbers 5904433, 5904441, 5904466, 7007755, 7008605, 7412807, 7413078, 7555365, 7555373, 7727717, and 7728350
Products Sold
model numbers 5904433, 5904441, 5904466, 7007755, 7008605, 7412807, 7413078, 7555365, 7555373, 7727717, and 7728350
Siemens Medical Solutions USA, Inc is recalling Axiom Artis X-Ray System using software version VB11D or VB20B due to Live display in exam room may sporadically stop working although the display in the control room remains fully operational. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Live display in exam room may sporadically stop working although the display in the control room remains fully operational
Recommended Action
Per FDA guidance
The manufacturer provided a Customer Safety Advisory letter dated 3/24/05. The letter describes the problem and the interim work around. This letter was forward to the recalling firm''s direct accounts.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, CT, FL, GA, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NJ, NY, NC, OH, OK, OR, PA, SC, TN, TX, VA, WA, WV, WI, DC
Page updated: Jan 10, 2026