Siemens recalls Luminos Agile Max model 10762472 due to risk of collision with obstacles or persons when using the bypass key override function. Affected units have specific serial numbers listed.
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 Agile Max medical imaging devices with model number 10762472. The issue involves a potential risk of collision with obstacles or people if the bypass key is used incorrectly to override the built-in collision control system.
The bypass key can override the built-in collision control system, which may cause the device to collide with obstacles or people when the operator uses the override function. This could lead to injuries if the device moves unexpectedly during medical procedures.
Medical professionals using the Luminos Agile Max for X-ray imaging are most at risk. Patients and staff in healthcare settings that use this specific model may also be affected.
Check for the model number 10762472 on the device. Affected units have specific serial numbers listed in the recall notice, including many numbers starting with 61000.
Review the bypass key settings to ensure it is not being used to override the built-in collision control system.
The model number is 10762472.
Affected units have specific serial numbers listed in the recall notice, including many numbers starting with 61000.
The recall notice does not mention a specific fix or remedy.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1332-2020 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1332-2020 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.
