Z-0316-2025 Class II Ongoing
FDA device recall Z-0316-2025 was initiated by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION on Sep 6, 2024 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 3.
Recall details
- Product Type
- Devices
- Report Date
- Nov 13, 2024
- Initiation Date
- Sep 6, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3
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.
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.
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.
Code information
UDI-DI: 04540217064809, 04540217064816. Serial Numbers: 41C3518D7001, 41C3518E4001, 41C3536D9001
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0316-2025
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026