SONIALVISION G4 recallZ-0316-2025 · Shimadzu Corporation Medical Systems Division · initiated Sep 6, 2024
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Shimadzu Corporation Medical Systems Division or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Software change control
What the company is doing
On 9/13/24, recall notices were emailed to consignees asking them to do the following: 1) If the problem occurs it is possible to solve this problem by turning off the power of the system and then pushing the reset switch on the Digital radiography unit s control cabinet. 2) Your firm authorized service representative will be contacting to schedule the implementation of the corrective action but if you are not contacted, contact the firm's National Support. 3) Complete and return the response form via email to response to [email protected] If you have questions contact the firm's National Technical Support at 844-487-2767, available 8:00AM-5:00PM, Monday - Friday.
Recall details
- Recall number
- Z-0316-2025
- Status
- Open, Classified
- Initiated by the company
- Sep 6, 2024
- Posted by the FDA
- Nov 7, 2024
- Recalling firm
- Shimadzu Corporation Medical Systems Division
- Quantity
- 3
- Product code
- JAA
- FDA submissions
- K190373
- Distribution
- US Nationwide distribution in the states of CA, CT, MA, WV, OH, NY, IA, NE, MN, IL, FL, NC, HI, LA, MD, MT, WA, AR, TX, TN, CO.
Product description
SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiographic and fluoroscopic examinations, including general radiography and pediatric examinations, excluding mammography.
Code information (models, lots, serial numbers)
UDI-DI: 04540217064809, 04540217064816. Serial Numbers: 41C3518D7001, 41C3518E4001, 41C3536D9001
Devices named in this recall
2 devices in the FDA device registry whose identifier appears in the recall's code information.
- SONIALVISION G4 503-78000-24Shimadzu Corporation · System, X-Ray, Fluoroscopic, Image-Intensified1 recall0 reports
- SONIALVISION G4 503-78000-54Shimadzu Corporation · System, X-Ray, Fluoroscopic, Image-Intensified1 recall0 reports
Product lines
Other products in the same recall event
The FDA groups related products into one recall event (event 95450).
- Z-0317-2025 · Open, ClassifiedThe FLUOROspeed is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a flat detector, it can perform a range of applicat…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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