Siemens UROSKOP Omnia Max: Resistor Overheating Risk
Siemens Medical recalls UROSKOP Omnia Max models with specific serial numbers due to resistor overheating that could ignite plastic housing. Affected units may need replacement.
Stop using this now
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Contact the company
What happened, in plain English
Siemens Medical is recalling UROSKOP Omnia Max ultrasound devices with model number 10762473 because a resistor in the frequency inverter can overheat and ignite the plastic housing. This poses a fire risk if the device is used normally. Read more at govinfonow.com/recall/52149-siemens-uroskop-omnia-max-resistor-overheating-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/52149-siemens-uroskop-omnia-max-resistor-overheating-risk · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1982-2025
Cite this page
“Siemens UROSKOP Omnia Max: Resistor Overheating Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/52149-siemens-uroskop-omnia-max-resistor-overheating-risk. Based on FDA recall #Z-1982-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1982-2025%22&limit=1).
Why it’s dangerous
A resistor in the frequency inverter can overheat significantly, potentially causing the plastic housing to catch fire. This fire hazard occurs during normal operation of the device, especially if the device is left running for extended periods without proper cooling.
Who’s affected
Users of the UROSKOP Omnia Max ultrasound device with model number 10762473 and specific serial numbers are affected. Healthcare professionals and medical facilities using this equipment are most at risk.
How to tell if you have this one
Check for model number 10762473 and serial numbers listed in the recall notice (e.g., 4014, 4056, 4049). The device is sold by Siemens Medical Solutions USA, Inc.
- Brand
Siemens Medical- Product
UROSKOP Omnia Max. Model Number: 10762473- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
Nationwide distribution.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1981-2025 | UROSKOP Omnia. Model Number: 10094910; Model Number: 10094910. No UDI. Serial Numbers: 3054, 3029, 3062, 3169, 3402, 3103, 3053, 3055, 3072, 3019, 3048, 3403, 3058, 1045, 2014, 3091, 3013, 3023, 3115, 3051, 3417, 3160, 2033, 3163, 3052, 3166, 3099, 3138, 3157, 3038, 3131, 3037, 3117, 3118, 3096, 3123, 3124, 2022, 2032, 2031, 3134, 3106, 3415, 3042, 3014, 3012, 3108, 3105, 3057, 2008, 3122, 3034, 3151, 3414, 2030, 3021, 3119, 3086, 3073, 3089, 3036, 3031, 3409, 3064, 3153, 3095, 3145, 3079, 3017, 3025, 3076, 2046, 2047, 2055, 2054, 2049, 3416, 2015, 1041, 3155, 3418, 3081, 3084, 2045, 3015, 3125, 3132, 3143, 3085, 3405, 2041, 2009, 3410, 2029, 3404. | 95 units |
| Z-1982-2025 | UROSKOP Omnia Max. Model Number: 10762473; Model Number: 10762473. UDI Numbers: (01)04056869008981(21)4014, (01)04056869008981(21)4056, (01)04056869008981(21)4049, (01)04056869008981(21)4015, (01)04056869008981(21)4063, (01)04056869008981(21)4022, (01)04056869008981(21)4036, (01)04056869008981(21)4043, (01)04056869008981(21)4024, (01)04056869008981(21)4059, (01)04056869008981(21)4020, (01)04056869008981(21)4032, (01)04056869008981(21)4053, (01)04056869008981(21)4061, (01)04056869008981(21)4060, (01)04056869008981(21)4051, (01)04056869008981(21)4025, (01)04056869008981(21)4037, (01)04056869008981(21)4054, (01)04056869008981(21)4042, (01)04056869008981(21)4033, (01)04056869008981(21)4055, (01)04056869008981(21)4052, (01)04056869008981(21)4047, (01)04056869008981(21)4062. Serial Numbers: 4014, 4056, 4049, 4015, 4063, 4022, 4036, 4043, 4024, 4059, 4020, 4032, 4053, 4061, 4060, 4051, 4025, 4037, 4054, 4042, 4033, 4055, 4052, 4047, 4062. | 25 units |
What to do — step by step
Stop Using It Now
Immediately stop using the UROSKOP Omnia Max device if it has the model number 10762473 and one of the listed serial numbers.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 21 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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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-1982-2025 (June 4, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1982-2025 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.