Merge Healthcare, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1762-2017)

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:

iConnect Enterprise Archive (ICEA) software. The firm name on the labeling is Merge Healthcare, Hartland, WI.

Product Classification:

Class II

Date Initiated: April 4, 2016

Date Posted: April 19, 2017

Recall Number: Z-1762-2017

Event ID: 76910

Reason for Recall:

An error message can occur resulting in the prior studies being unavailable for viewing.

Status: Terminated

Product Quantity: 333 sites potentially have the affected versions

Code Information:

Versions : 8.30, 8.30.2, 8.40.0, 8.40.1, 8.40.1 HF0557, 8.40.s, 8.40.2.1, 8.40.2.2, 8.80, 8.80.0.1, 8.80.1.1, 8.80.2, 8.80.0.2, 9.0.0, 9.0.0.1, 9.1.0, 9.1.1, 9.1.2, 9.1.2.1, 9.1.2.2, 9.2.0, 9.3.0, 9.3.1, 9.4.0, 9.4.1, 9.4.2, 9.4.2.1., and 9.4.3

Distribution Pattern:

Distribution was made nationwide to medical facilities. Foreign distribution was made to Canada, as well as other countries. Government/military distribution was also made.

Voluntary or Mandated:

Voluntary: Firm initiated