Siemens Medical Solutions recalls interventional fluoroscopic x-ray systems due to rare risk of incorrect high dose reporting. Affected models include 4056869149325. No remedy specified in recall notice.
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
Siemens Medical Solutions is recalling certain interventional fluoroscopic x-ray systems because they may incorrectly report high radiation doses in very rare situations. This could potentially lead to unnecessary radiation exposure during procedures.
The system's sensor and software may fail to communicate in very rare situations, causing it to report a high radiation dose when none was actually applied. This could lead to unnecessary radiation exposure during medical procedures.
Healthcare professionals using the recalled x-ray systems are most at risk. Patients undergoing procedures with these systems may also be affected.
The recalled system has the model number 405:6869149325. This x-ray system was sold by Siemens Medical Solutions.
Look for the model number 4056869149325 on the system.
The recall notice does not specify any remedy.
Check for the model number 4056869149325 on the system.
The recall notice does not specify any action steps.
We’ve drafted a message you can send Siemens Medical Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-2022-2025 — Siemens Medical Solutions Siemens Medical Solutions Hello, I own a Siemens Medical Solutions that is covered by recall Z-2022-2025 from Siemens Medical Solutions. 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.
