Reported Jun 25, 2025 · Ongoing

UROSKOP Omnia. Model Number: 10094910

Siemens Medical Solutions USA, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Siemens Medical Solutions USA, Inc · 40 Liberty Blvd · Malvern, PA · 19355-1418

Is this the product you have?

  • UROSKOP Omnia
  • Model Number10094910
Lot codes and dates
  • Model Number10094910. No UDI
  • Serial Numbers

    95 of 95 codes

    • 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
Amount recalled
95 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.