Siemens Medical Solutions USA, Inc SIEMENS AXIOM Artis - AUTOMAP FUNCTION Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SIEMENS AXIOM Artis - AUTOMAP FUNCTION
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
10052, 10055, 10064, 10072, 10086, 10094, 10124, 10148, 10151, 10153, 10176, 10177, 10182, 10198, 10217, 10228, 10237, 10240, 10243, 10249, 10251, 10253, 10266, 10284, 10298, 10307, 10326, 10335, 10338, 10348, 10364, 10365, 10367, 10369 AXIOM Artis BC: 14007 AXIOM Artis MP: 20022, 20024, 20032, 20036, 20045, 20048, 20070, 20078, 20082, 20090, 20094, 20107, 20110, 20111, 20155, 20169, 20177, 20190, 20199, 20203, 20205
Products Sold
Model Numbers: AXIOM Artis FC 5904433 AXIOM Artis BC 5904649 AXIOM Artis MP 5904466 AXIOM Artis FA 5904441 AXIOM Artis BA 5904656 AXIOM Artis TA 7007755 AXIOM Artis FC: 10050; 10052; 10055; 10064; 10072; 10086; 10094; 10124; 10148; 10151; 10153; 10176; 10177; 10182; 10198; 10217; 10228; 10237; 10240; 10243; 10249; 10251; 10253; 10266; 10284; 10298; 10307; 10326; 10335; 10338; 10348; 10364; 10365; 10367; 10369 AXIOM Artis BC: 14007 AXIOM Artis MP: 20022; 20024; 20032; 20036; 20045; 20048; 20070; 20078; 20082; 20090; 20094; 20107; 20110; 20111; 20155; 20169; 20177; 20190; 20199; 20203; 20205
Siemens Medical Solutions USA, Inc is recalling SIEMENS AXIOM Artis - AUTOMAP FUNCTION due to Error appears in the AUTOMAP function, Module 2, when PERISTEEPING or PERIVISION is activated simultaneously that causes system to crash.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Error appears in the AUTOMAP function, Module 2, when PERISTEEPING or PERIVISION is activated simultaneously that causes system to crash.
Recommended Action
Per FDA guidance
The recalling firm sent recall letter to their customers informing them of the software problem. The customers were informed that a Siemens Service Representative will visit each location to deactivate Module 2 of the AUTOMAP function per Update AX023/04S.
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