Reported Jun 25, 2025 · Ongoing
UROSKOP Omnia Max. Model Number: 10762473
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 Max
- Model Number10762473
- Lot codes and dates
- Model Number10762473
- 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
4014405640494015406340224036404340244059402040324053406140604051402540374054404240334055405240474062
- Amount recalled
- 25 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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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