FDA Enforcement Class II Terminated

Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical character recognition of measurements captured on images) and cardiology signal (waveform) data.

Recall: Z-1046-2017 · Reported January 25, 2017

Enforcement

Recall Number
Z-1046-2017
Event ID
75957
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Merge Healthcare, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
January 25, 2017
Initiation Date
March 28, 2016
Classification Date
January 18, 2017
Termination Date
April 8, 2019
Address
900 Walnut Ridge Dr, Hartland, WI, 53029-8347, United States

Description

Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical character recognition of measurements captured on images) and cardiology signal (waveform) data.

Reason

If a reader selects Multi-study review prior to the original study completing its loading process and then immediately returns to image review of the original study, it is possible that not all current images will be present for review, which could result in incorrect treatment/diagnosis.

Code Info

Versions: 9.0, 9.0.1, 9.0.2, 9.0.3, 9.0.4, 9.0.5, 9.0.6, 9.0.7, 9.0.8, 9.0.9, 10.0, 10.0.1, 10.1, 10.1.1, and 10.1.2

Distribution

US Nationwide Distribution

Quantity

188 sites potentially have the effected versions