Siemens AXIOM Luminos Agile Footrest May Detach During Use

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Recalling firmSiemens Medical Solutions USA, Inc40 Liberty Blvd, N/A · 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 AXI:OM Luminos Agile patient tables because the footrest might detach while in use. This could lead to injury if the table becomes unstable. Affected units have specific serial numbers and material codes.

Why it’s dangerous

The footrest may detach from the patient table during use, potentially causing the table to become unstable. This could lead to injury if the patient or staff falls or is struck by the moving table.

Who’s affected

Healthcare facilities using Siemens AXIOM Luminos Agile patient tables are most at risk. Patients and staff could be injured if the footrest detaches during procedures.

How to tell if you have this one

Check for the specific serial numbers and material code 10502200 listed in the recall notice. The product is sold under the brand name Siemens Medical Solutions.

Brand
Siemens
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the serial number and material code 10502200 to confirm if your unit is affected.

✎ GovInfoNow

Questions people ask

Is this recall affecting my patient table?

The recall applies to Siemens AXIOM Luminos Agile patient tables with specific serial numbers and material code 10502200. Check your unit's details to confirm.

What should I do if I have this table?

The recall does not specify a remedy, so contact Siemens directly to confirm if your unit is affected and get guidance.

How can I tell if my table is affected?

Look for the serial number and material code 10502200 on your unit. Affected units are identified by these specific details.

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-1001-2023 — Siemens Siemens

Hello,

I own a Siemens that is covered by recall Z-1001-2023 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-1001-2023 (December 9, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1001-2023 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 Luminos Agile

Use caution until it’s fixed