PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: November 23, 2016 Initiated: May 25, 2016 #Z-0611-2017

Product Description

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

Reason for Recall

Software displayed incorrect prior reports in the viewport area, only when more than one prior study (2 or more) was viewed.

Details

Recalling Firm
Merge Healthcare, Inc.
Units Affected
60 sites potentially have the affected versions
Distribution
Distribution was made to medical facilities nationwide. Foreign distribution was also made.
Location
Hartland, WI

Frequently Asked Questions

What product was recalled?
iConnect Access software. The firm name on the label is Merge Healthcare, Hartland, WI.. Recalled by Merge Healthcare, Inc.. Units affected: 60 sites potentially have the affected versions.
Why was this product recalled?
Software displayed incorrect prior reports in the viewport area, only when more than one prior study (2 or more) was viewed.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 23, 2016. Severity: Moderate. Recall number: Z-0611-2017.