Merge Healthcare, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2590-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Merge PACS software. The firm name on the label is Merge Healthcare, Hartland, WI.

Product Classification:

Class II

Date Initiated: May 8, 2017

Date Posted: June 21, 2017

Recall Number: Z-2590-2017

Event ID: 77248

Reason for Recall:

Merge PACS did not show unviewed images when the last view was skipped. There is a potential risk to health of a physician misdiagnosis because not all images are available for viewing.

Status: Terminated

Product Quantity: 47 sites potentially have the affected versions

Code Information:

Versions 7.0.2.1, 7.0.2.2, 7.0.2.3, 7.0.2.3 P1, and 7.0.2.3 P2

Distribution Pattern:

USA (nationwide) Distribution .There was no foreign/government/military distribution.

Voluntary or Mandated:

Voluntary: Firm initiated