Siemens Medical Solutions USA, Inc Axiom Artis MP X-Ray System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Axiom Artis MP X-Ray System
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Serial numbers 10, 1021, 1025, 1026, 1027, 1043, 1044, 1048, 1050, 1052, 1056, 1065, 1067, 1069, 1080, 1082, 1083, 1085, 1087, 1089, and 1097.
Products Sold
Serial numbers 10, 1021, 1025, 1026, 1027, 1043, 1044, 1048, 1050, 1052, 1056, 1065, 1067, 1069, 1080, 1082, 1083, 1085, 1087, 1089, and 1097.
Siemens Medical Solutions USA, Inc is recalling Axiom Artis MP X-Ray System due to potential problem with the fluoroscopy switch on the power grip. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
potential problem with the fluoroscopy switch on the power grip
Recommended Action
Per FDA guidance
The recalling firm''s Customer Service Engineers are visiting each account to correct/replace the Power Grip button.
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, DE, IN, IA, MI, NE, NC, PA, RI, TX, WA, WI, DC
Page updated: Jan 10, 2026