Merge Healthcare, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2620-2017)

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.

Product Classification:

Class II

Date Initiated: May 24, 2017

Date Posted: June 28, 2017

Recall Number: Z-2620-2017

Event ID: 77265

Reason for Recall:

A migrated study that has annotations will display the annotations, but when a prior study is loaded that should have annotations, the second study will not display annotations.

Status: Terminated

Product Quantity: 98 sites potentially have the affected versions

Code Information:

Versions 6.6, 6.6.1, and 6.6.2

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated