Merge Healthcare, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2601-2017)

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

Product Classification:

Class II

Date Initiated: May 24, 2017

Date Posted: June 28, 2017

Recall Number: Z-2601-2017

Event ID: 77271

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: 160 sites potentially have the affected versions

Code Information:

Versions 6.6, 6.6.1, 6.6.2, 6.6.2.1, and 6.6.2.2

Distribution Pattern:

USA (nationwide) Distribution was made to medical facilities. There was no foreign/government/military distribution.

Voluntary or Mandated:

Voluntary: Firm initiated