Siemens Medical recalls UROSKOP Omnia Max models with specific serial numbers due to resistor overheating that could ignite plastic housing. Affected units may need replacement.
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Siemens Medical is recalling UROSKOP Omnia Max ultrasound devices with model number 10762473 because a resistor in the frequency inverter can overheat and ignite the plastic housing. This poses a fire risk if the device is used normally.
A resistor in the frequency inverter can overheat significantly, potentially causing the plastic housing to catch fire. This fire hazard occurs during normal operation of the device, especially if the device is left running for extended periods without proper cooling.
Users of the UROSKOP Omnia Max ultrasound device with model number 10762473 and specific serial numbers are affected. Healthcare professionals and medical facilities using this equipment are most at risk.
Check for model number 10762473 and serial numbers listed in the recall notice (e.g., 4014, 4056, 4049). The device is sold by Siemens Medical Solutions USA, Inc.
Immediately stop using the UROSKOP Omnia Max device if it has the model number 10762473 and one of the listed serial numbers.
Model number 10762473 with specific serial numbers listed in the recall notice (e.g., 4014, 4056, 4049).
Check the device's model number and serial numbers against the list provided in the recall notice.
Immediately stop using it and contact Siemens Medical Solutions USA, Inc for further instructions.
We’ve drafted a message you can send Siemens Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1982-2025 — Siemens Medical Siemens Medical Hello, I own a Siemens Medical that is covered by recall Z-1982-2025 from Siemens Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
