FUJIFILM recalls software version v7.4.310 for inaccurate ruler measurements in radiological image processing systems. Affected units include specific serial numbers and UDI codes.
Software issue may cause the ruler measurement to be inaccurate.
FUJIFILM is recalling a specific version of its Synapse PACS software due to potential inaccuracies in ruler measurements. This could lead to incorrect medical imaging measurements if the software is used in radiology systems.
The software issue causes ruler measurements to be inaccurate, which could result in incorrect medical imaging data. This might affect patient treatment decisions if measurements are critical for diagnosis or treatment planning.
Healthcare facilities using the recalled software version v7.4.310 for radiological imaging are affected. Medical professionals handling the software are most at risk of measurement errors.
Check for the software version v7.4.310 on your radiological image processing system. Affected units have specific serial numbers and UDI codes listed in the recall notice.
Verify your software version is v7.4.310 by checking the system settings or documentation.
The recall states ruler measurements may be inaccurate, but it does not specify patient harm. The official notice does not mention patient injury risks.
Check the software version number; affected units are v7.4.310 with specific serial numbers and UDI codes listed in the recall notice.
The recall does not provide a remedy, so users should check the software version and contact FUJIFILM Healthcare Americas Corporation for further guidance.
We’ve drafted a message you can send FUJIFILM to request your refund or repair — edit it as you like.
Subject: Recall Z-3030-2026 — FUJIFILM FUJIFILM Hello, I own a FUJIFILM that is covered by recall Z-3030-2026 from FUJIFILM. 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.
