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.

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.