--- title: "UROSKOP Omnia. Model Number: 10094910 — FDA record Z-1981-2025 | Is It on Recall" description: "A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire." url: https://isitonrecall.com/recall/fda-device-z-1981-2025-uroskop-omnia-model-number-10094910/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # UROSKOP Omnia. Model Number: 10094910 — FDA record Z-1981-2025 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Jun 4, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: UROSKOP Omnia. Model Number: 10094910 - **Reason**: A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire. - **Classification**: Class II - **Recalling firm**: Siemens Medical Solutions USA, Inc - **Quantity**: 95 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-1981-2025 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1981-2025%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | 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. | Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution Nationwide distribution. States below are derived from the distribution text, including nationwide wording. 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These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1981-2025%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Siemens Medical Solutions USA, Inc records](https://isitonrecall.com/brand/siemens-medical-solutions-usa-inc/)