Siemens recalls Luminos dRF Max model 10762471 due to risk of collision with obstacles or persons when using the bypass key override function.
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 Luminos dRF Max medical imaging devices with model number 10762471. The recall is because using the bypass key override function can cause the device to collide with obstacles or people, creating a safety risk during medical procedures.
The bypass key override function can be incorrectly used, bypassing the built-in collision control system. This may cause the device to move unexpectedly and collide with obstacles or people during medical imaging procedures.
Medical professionals using the Luminos dRF Max device for imaging procedures are most at risk. Patients and staff near the device during operation could also be affected if collisions occur.
Check for the model number 10762471 on the device. The recall includes specific serial numbers listed in the official notice.
Verify the model number on the device to confirm if it is 10762471.
Ensure proper use of the bypass key override function to avoid bypassing collision controls.
The recalled model number is 10762471.
Incorrect use of the bypass key override function can cause the device to collide with obstacles or people.
Check the model number on the device; the recall includes specific serial numbers listed in the official notice.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1331-2020 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1331-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
