PlainRecalls
FDA Devices Moderate Class II Terminated

Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.

Reported: October 24, 2018 Initiated: August 30, 2018 #Z-0195-2019

Product Description

Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.

Reason for Recall

Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present.

Details

Recalling Firm
GE Healthcare, LLC
Units Affected
1
Distribution
NY
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.. Recalled by GE Healthcare, LLC. Units affected: 1.
Why was this product recalled?
Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 24, 2018. Severity: Moderate. Recall number: Z-0195-2019.