PlainRecalls
FDA Devices Moderate Class II Terminated

Merge Unity software, formerly known as DR Systems Unity PACS software. The firm name on the label is Merge Healthcare, Hartland, WI. Merge Unity is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a variety of diagnostic imaging systems

Reported: September 13, 2017 Initiated: August 14, 2017 #Z-3105-2017

Product Description

Merge Unity software, formerly known as DR Systems Unity PACS software. The firm name on the label is Merge Healthcare, Hartland, WI. Merge Unity is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a variety of diagnostic imaging systems

Reason for Recall

The software is not identifying the patient as having atypical hyperplasia, resulting in an incorrect Gail Risk calculation.

Details

Recalling Firm
Merge Healthcare, Inc.
Units Affected
98 sites have the potentially affected software
Distribution
Nationwide Distribution
Location
Hartland, WI

Frequently Asked Questions

What product was recalled?
Merge Unity software, formerly known as DR Systems Unity PACS software. The firm name on the label is Merge Healthcare, Hartland, WI. Merge Unity is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a variety of diagnostic imaging systems. Recalled by Merge Healthcare, Inc.. Units affected: 98 sites have the potentially affected software.
Why was this product recalled?
The software is not identifying the patient as having atypical hyperplasia, resulting in an incorrect Gail Risk calculation.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 13, 2017. Severity: Moderate. Recall number: Z-3105-2017.