Siemens recalls AXIOM MULTIX MP X-ray tables due to potential fire from power supply short circuits. Affected models include specific serial numbers; stop using immediately to prevent fire risk.
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Siemens is recalling AXIOM MULTIX MP X-ray tables that could overheat and catch fire due to a power supply short circuit. This hazard requires immediate action to avoid fire risks.
The power supply unit in the touch display can short circuit, causing overheating and potentially starting a fire. This risk occurs when the table is in normal use without proper maintenance.
Healthcare facilities using Siemens AXIOM MULTIX MP X-ray tables with the listed serial numbers are most at risk. Patients and staff could face fire hazards if the table is used without correction.
Check for serial numbers listed: 1004, 1006, 1051, 1062, 1172, 1173, 1175, 1179, 1180, 1181, 1184, 1186, 1187, 1193, 1198, 1200, 1202, 1204, 1205, 1206. The table is used with Siemens Multix PRO and TOP Systems radiographic devices.
Immediately stop using the affected X-ray table to prevent fire risk from overheating.
The recalled model is Siemens AXIOM MULTIX MP X-ray table used with Siemens Multix PRO and TOP Systems radiographic devices.
Check for serial numbers listed: 1004, 1006, 1051, 1062, 1172, 1173, 1175, 1179, 1180, 1181, 1184, 1186, 1187, 1193, 1198, 1200, 1202, 1204, 1205, 1206.
The recall record does not mention a remedy or replacement option.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2183-2024 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2183-2024 from Siemens. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.