Siemens UROSKOP Omnia Device May Overheat and Ignite - Recall

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Siemens is recalling UROSKOP Omnia devices with model number 10094910 because a resistor in the frequency inverter can overheat and potentially ignite the plastic housing, causing a fire. This recall affects specific units with listed serial numbers.

Why it’s dangerous

A resistor in the frequency inverter can overheat significantly, which may cause the plastic housing to catch fire. This fire hazard could lead to serious injury or property damage if the device is in use.

Who’s affected

Users of the UROSKOP Omnia device with model number 10094910 and specific serial numbers listed in the recall notice are affected. Medical professionals who use this device for imaging are at the highest risk.

How to tell if you have this one

Check the model number on the device, which should be 10094910. Affected units have specific serial numbers listed in the recall notice, including 3054, 3029, 3062, and other numbers provided in the record.

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 UROSKOP Omnia device with model number 10094910 if it has one of the listed serial numbers.

✎ GovInfoNow

Questions people ask

What model number is affected by this recall?

The affected model number is 10094910.

How can I check if my device is affected?

Check the model number on the device and compare it to 10094910. Affected units have specific serial numbers listed in the recall notice.

What should I do if I have the affected device?

Immediately stop using the device and contact Siemens for further instructions.

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-1981-2025 — Siemens Siemens

Hello,

I own a Siemens that is covered by recall Z-1981-2025 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-1981-2025 (June 4, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1981-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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 UROSKOP Omnia. Model Number: 10094910

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