Merge Healthcare, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1431-2017)

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.

Product Classification:

Class II

Date Initiated: April 4, 2016

Date Posted: March 15, 2017

Recall Number: Z-1431-2017

Event ID: 76594

Reason for Recall:

Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate via telmed protocol to the destination server and may fail to import on the destination server.

Status: Terminated

Product Quantity: 248 sites potentially have the affected versions

Code Information:

Versions 6.6.1, 6.6.1.1, 6.6.2, 6.6.2.1, 6.6.2.2, 7.0, and 7.0.1

Distribution Pattern:

USA (nationwide ) Distribution was made to medical facilities. Internationally to Canada. There was no government or military distribution.

Voluntary or Mandated:

Voluntary: Firm initiated