FDA recall Z-0232-2018

Fujifilm Medical Systems U.S.A., Inc. · Class II · device

Product

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 all routine radiography examinations.

Reason for recall

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.

Distribution

US Distribution.

Key facts

Status
Terminated
Initiation date
2017-06-15
Report date
2017-12-20
Termination date
2018-05-09
Voluntary/Mandated
Voluntary: Firm initiated
Location
Stamford, CT, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0232-2018