FUJIFILM Synapse PACS Software v7.4.310: Inaccurate Ruler Measurements
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.
Lower-risk recall
Software issue may cause the ruler measurement to be inaccurate.
What happened, in plain English
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. Read more at govinfonow.com/recall/697854-fujifilm-synapse-pacs-software-v7-4-310-inaccurate-ruler-measurements.
Source Summary by GovInfoNow · govinfonow.com/recall/697854-fujifilm-synapse-pacs-software-v7-4-310-inaccurate-ruler-measurements · Updated September 14, 2026 · FDA enforcement record: FDA #Z-3030-2026
Cite this page
“FUJIFILM Synapse PACS Software v7.4.310: Inaccurate Ruler Measurements.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/697854-fujifilm-synapse-pacs-software-v7-4-310-inaccurate-ruler-measurements. Based on FDA recall #Z-3030-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3030-2026%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
FUJIFILM- Product
FUJIFILM Synapse PACS software v7.4.310; radiological image processing system- Category
Medical device
What to do — step by step
Check Software Version
Verify your software version is v7.4.310 by checking the system settings or documentation.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 5 states.
FDA distribution: “Worldwide - US Nationwide distribution in the states of NY, VA, KS, OR, OH, and the country of Australia.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Kansas, New York, Ohio, Oregon, Virginia.
Recall timeline
FDA published this recall 42 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-3030-2026 (July 22, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3030-2026 to see it in context.
- Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.