Siemens Medical Solutions USA, Inc Axiom Aristos MX/VX. Model number 58 95 003 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Axiom Aristos MX/VX. Model number 58 95 003
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Serial numbers 1001 through 1017, 1019 through 1071, and 1073 through 1469
Products Sold
Serial numbers 1001 through 1017, 1019 through 1071, and 1073 through 1469
Siemens Medical Solutions USA, Inc is recalling Axiom Aristos MX/VX. Model number 58 95 003 due to potential issue (system may lock up) when repeating patient registrations. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
potential issue (system may lock up) when repeating patient registrations
Recommended Action
Per FDA guidance
The recalling firm issed a Customer Advisory Letter via certified mail to their cutomers informing them of the problem and information for the workaround to prevent problems for occurring until the software is upgraded.
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 noticePage updated: Jan 10, 2026