SONIALVISION G4Recalls & reported problems across all models
Shimadzu Corporation · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one SONIALVISION G4 model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of SONIALVISION G4 by Shimadzu Corporation in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
SONIALVISION G4 recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Sep 6, 2024Open, Classified
X-ray R/F system software with certain versions of the control board may occasionally fail to display images when switching from Fluoroscopy mode to Radiography mode, which may lead to the possibility of delay or cancellation of the examination.
Z-0316-2025 · Root cause: Software change control · names 2 of these models · Recall details · FDA record ↗
SONIALVISION G4 models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- SONIALVISION G4 503-78000-24System, X-Ray, Fluoroscopic, Image-Intensified1 recall0 reports
- SONIALVISION G4 503-78000-54System, X-Ray, Fluoroscopic, Image-Intensified1 recall0 reports
Other Shimadzu Corporation products
All Shimadzu Corporation devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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