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
305430293062316934023103305330553072301930483403305810452014309130133023311530513417316020333163305231663099313831573038313130373117311830963123312420222032203131343106341530423014301231083105305720083122303431513414203030213119308630733089
- 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.
Want the full recall guide?
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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