SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION: Device Recall
Recall #Z-0316-2025 · 09/06/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0316-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
- Status
- Ongoing
- Date Initiated
- 09/06/2024
- Location
- Kyoto, N/A, Japan
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3
Reason for Recall
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.
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.
Distribution Pattern
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.
Other Recalls by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
- Class II: Risk 10/16/2025
- Class II: Risk 09/06/2024
- Class II: Risk 09/06/2024
View all recalls by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION →
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.