Fujifilm Medical Systems U.S.A., Inc.: Medical Device Recall in 2019 - (Recall #: Z-2441-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Fujifilm FDR Go Plus mobile X-ray system

Product Classification:

Class II

Date Initiated: July 19, 2019

Date Posted: September 11, 2019

Recall Number: Z-2441-2019

Event ID: 83524

Reason for Recall:

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

Status: Terminated

Product Quantity: 174 units

Code Information:

All serial numbers

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated