Fujif: FDR Go Plus Mobile X-Ray System May Show Blue Screen of Death
Fujifilm recalls FDR Go Plus mobile X-ray systems due to potential Blue Screen of Death errors. Affected units have all serial numbers.
Lower-risk recall
The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)
Contact the company
What happened, in plain English
Fujifilm is recalling its FDR Go Plus mobile X-ray systems because a software issue might cause a Blue Screen of Death error. This could disrupt medical imaging operations and delay patient care. Read more at govinfonow.com/recall/67387-fujif-fdr-go-plus-mobile-x-ray-system-may-show.
Source Summary by GovInfoNow · govinfonow.com/recall/67387-fujif-fdr-go-plus-mobile-x-ray-system-may-show · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2441-2019
Cite this page
“Fujif: FDR Go Plus Mobile X-Ray System May Show Blue Screen of Death.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67387-fujif-fdr-go-plus-mobile-x-ray-system-may-show. Based on FDA recall #Z-2441-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2441-2019%22&limit=1).
Why it’s dangerous
The graphics driver in the FDR Go Plus might cause the system to display a Blue Screen of Death error. This error could interrupt medical imaging procedures and delay patient care without causing physical harm.
Who’s affected
Healthcare facilities using the FDR Go Plus mobile X-ray system are affected. Medical staff and patients using this equipment may experience temporary disruptions.
How to tell if you have this one
The FDR Go Plus mobile X-ray system with any serial number is affected. This recall covers all units sold by Fujifilm Medical Systems U.S.A., Inc.
- Brand
Fujifilm- Category
Medical device
What to do — step by step
Check Serial Number
Verify the serial number on your FDR Go Plus mobile X-ray system to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using the device immediately?
The recall does not require immediate discontinuation of use; the hazard level is low risk.
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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-2441-2019 (July 19, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2441-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 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.