Siemens AXIOM MULTIX MP X-ray Table Recall: Fire Risk from Power Supply Short Circuit

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Contact the company & request your remedy

Recalling firmSiemens Medical Solutions USA, Inc40 Liberty Blvd · Malvern, PA 19355-1418

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Siemens is recalling AXIOM MULTIX MP X-ray tables that could overheat and catch fire due to a power supply short circuit. This hazard affects medical facilities using these tables with Siemens Multix PRO systems.

Why it’s dangerous

A short circuit in the power supply unit can cause overheating, which may lead to fire. This hazard occurs when the touch display is powered on and the short circuit is active.

Who’s affected

Medical facilities using Siemens AXIOM MULTIX MP X-ray tables with Multix PRO systems are most at risk. Patients and staff could be affected if the table malfunctions during use.

How to tell if you have this one

Check for serial numbers: 1022, 1074, 1118, 1119, 1120, 1121, 1123, 1126, 1130, 1131, 1134, 1138. The table is used with Siemens Multix PRO and TOP Systems radiographic devices.

Brand
Siemens
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Numbers
Look for the specific serial numbers listed: 1022, 1074, 1118, 1119, 1120, 1121, 1123, 1126, 1130, 1131, 1134, 1138.

✎ GovInfoNow

Questions people ask

Why is this X-ray table being recalled?

The power supply unit in the touch display may short circuit, causing overheating and fire risk.

What should I do if I have this table?

The recall record does not specify a remedy, so contact Siemens directly for guidance.

Is this table safe to use?

The recall indicates a fire risk, so it is not safe to use until the issue is resolved.

Take action

Contact Siemens

We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2182-2024 — Siemens Siemens

Hello,

I own a Siemens that is covered by recall Z-2182-2024 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.

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Where this comes from

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.

Official source: FDA Recall #Z-2182-2024 (May 31, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2182-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Siemens Medical Solutions USA, Inc recalls AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO

Use caution until it’s fixed