FDA recall Z-2441-2019

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

Product

Fujifilm FDR Go Plus mobile X-ray system

Reason for recall

The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2019-07-19
Report date
2019-09-11
Termination date
2020-08-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lexington, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2441-2019