Siemens recalls Uroskop Omnia Max model 10762473 due to risk of collision with obstacles or persons when using the bypass key override function incorrectly.
Siemens became aware of an issue of incorrect use of the bypass key overriding the built-in collision control creating risk of collision with obstacles or persons when the operator uses the override function.
Siemens is recalling Uroskop Omnia Max ultrasound devices with model number 10762473 because incorrect use of the bypass key can override collision controls, potentially causing collisions with people or objects. This could lead to injury if the device is used improperly.
The bypass key can override the built-in collision control system, which is designed to prevent the device from colliding with obstacles or people. If the operator uses the override function incorrectly, the device may move into contact with unintended objects or individuals, potentially causing injury.
Urology professionals and healthcare facilities using Siemens Uroskop Omnia Max devices with model number 10762473 are affected. Those who use the bypass key override function without proper training or awareness are at higher risk.
Check for the model number 10762473 on the device. The serial numbers listed in the recall include a range of numbers starting with 4000 to 4664.
Read the device's manual to understand the correct use of the bypass key and collision control system to avoid accidental collisions.
The recalled model number is 10762473.
Check the model number on the device; affected units have model number 10762473 with specific serial numbers listed in the recall.
Review the device instructions to ensure correct use of the bypass key and collision controls to prevent potential collisions.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1333-2020 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1333-2020 from Siemens. 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.
