UROSKOP Omnia Max recalled over fire hazard
- Recall date
- June 4, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Siemens Medical Solutions USA, Inc recalls UROSKOP Omnia Max. Model Number: 10762473
- Recall number
- Z-1982-2025
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- Nationwide distribution.
Why it was recalled
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
UROSKOP Omnia Max. Model Number: 10762473
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