Siemens Medical Solutions USA, Inc Axiom Artis dMP, Axiom Artis Modular Angiography X-Ray System, Model number 7555365. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Axiom Artis dMP, Axiom Artis Modular Angiography X-Ray System, Model number 7555365.
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Model number 7555365. Serial numbers: 57001, 57002, 57093, 57103, 57119, 57122, 57132, 57133, 57134, 57135, 57136, 57137, 57139, 57140, 57141, 57143, 57144, 57145, 57146, 57147, 57148, 57149, 57150, 57151, 57152, 57153, 57154, 57156, 57157, 57158, 57159, 57160, 57161, 57162, 571 63, 57164, 57165, 57166, 57167, 57168, 57169, 57170, 57171, 57172, 57173, 57174, 57175, 57177, 57178, 57179, 57181, 57182, 57183, 57184, 57185, and 57186
Products Sold
Model number 7555365. Serial numbers: 57001, 57002, 57093, 57103, 57119, 57122, 57132, 57133, 57134, 57135, 57136, 57137, 57139, 57140, 57141, 57143, 57144, 57145, 57146, 57147, 57148, 57149, 57150, 57151, 57152, 57153, 57154, 57156, 57157, 57158, 57159, 57160, 57161, 57162, 571 63, 57164, 57165, 57166, 57167, 57168, 57169, 57170, 57171, 57172, 57173, 57174, 57175, 57177, 57178, 57179, 57181, 57182, 57183, 57184, 57185, and 57186
Siemens Medical Solutions USA, Inc is recalling Axiom Artis dMP, Axiom Artis Modular Angiography X-Ray System, Model number 7555365. due to Incorrect contour finding: Image may be calibrated to the wrong size catheter.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect contour finding: Image may be calibrated to the wrong size catheter.
Recommended Action
Per FDA guidance
Siemens issued a Customer Safety Advisory Notice dated 8/29/08 to inform customers of the potential issue. The recalling firm issued Update Instructions AX040/08/S to the service engineers which provides information to fix the problem.
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