Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0232-2018 — FUJIFILM FDR Visionary Suite with CH-200. Model # CH-200, Catalog: Visionary Suite (FMSU Marketing Name) The FDR Visionary Suite is intended to generate digital or conventional radiographic images of the skull, spinal column, chest, abdomen, extremities, and other body parts of human anatomies in

U.S. FDA — Device Enforcement · United States · 2017-06-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0232-2018
Date of alert
2017-06-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Fujifilm Medical Systems U.S.A., Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04540217052226
Reported risk: A potential issue in the X-ray tube ceiling unit CH-200 which constitutes the Digital Radiography System FDR Visionary Suite. The X-ray tube assembly in these devices is mounted to a tube mounting flange, which is part of the tube holding shaft. where cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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