PlainRecalls
FDA Devices Moderate Class II Terminated

Merge Cardio software.

Reported: March 29, 2017 Initiated: April 4, 2016 #Z-1486-2017

Product Description

Merge Cardio software.

Reason for Recall

Cardio study list does not show STAT studies without refreshing.

Details

Recalling Firm
Merge Healthcare, Inc.
Units Affected
217 sites potentially have the affected versions
Distribution
Distribution was nationwide to medical facilities. There was also military distribution. There was no foreign/government distribution.
Location
Hartland, WI

Frequently Asked Questions

What product was recalled?
Merge Cardio software.. Recalled by Merge Healthcare, Inc.. Units affected: 217 sites potentially have the affected versions.
Why was this product recalled?
Cardio study list does not show STAT studies without refreshing.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 29, 2017. Severity: Moderate. Recall number: Z-1486-2017.