Merge Healthcare, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0294-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Fusion Workstation.; Indicated for the transmission and review of radiological images.

Product Classification:

Class II

Date Initiated: October 28, 2011

Date Posted: October 26, 2016

Recall Number: Z-0294-2017

Event ID: 75425

Reason for Recall:

After a period of time running Fusion Workstation, the Hounsfield measurement tool will report incorrect values.

Status: Terminated

Product Quantity: 13 sites potentially hae the affected version

Code Information:

Versions V3.0.2 P3, 3.02, 3.1, 3.2, 3.3, and 3.3.1.

Distribution Pattern:

Distribution was made to AZ, CA, ID, IL, IN, MI, MN, and NJ.

Voluntary or Mandated:

Voluntary: Firm initiated