Siemens Multix TOP I PRO 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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Siemens is recalling specific Multix TOP I PRO X-ray tables that could overheat and start a fire due to a power supply short circuit. This recall affects hospitals and clinics using these tables with Siemens Multix PRO and TOP systems.

Why it’s dangerous

The power supply unit in the Touch Display can short circuit, causing overheating and potentially starting a fire. This hazard occurs during normal use when the table is powered on.

Who’s affected

Hospitals and clinics using the affected Multix TOP I PRO X-ray tables with Siemens Multix PRO and TOP systems are most at risk. The recall applies to units with specific serial numbers.

How to tell if you have this one

Check the serial number on the table. Affected units have serial numbers 1004, 1006, 1011, or 1014. The table is used with Siemens Multix PRO and TOP radiographic systems.

Brand
Siemens
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using It Now
Immediately stop using the affected Multix TOP I PRO X-ray table as it poses a fire risk.

✎ GovInfoNow

Questions people ask

What is the specific model of X-ray table being recalled?

The recalled model is the Siemens Multix TOP I PRO Radiographic X-ray Table.

What serial numbers are affected?

Serial numbers 1004, 1006, 1011, and 1014 are affected.

How can I check if my table is affected?

Check the serial number on the table; affected units have serial numbers 1004, 1006, 1011, or 1014.

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-2186-2024 — Siemens Siemens

Hello,

I own a Siemens that is covered by recall Z-2186-2024 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-2186-2024 (May 31, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2186-2024 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 MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with

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