Recall Z-1333-2022— GE Healthcare, LLC

Name: FDA recall Z-1333-2022
Creator: U.S. Food and Drug Administration
Published: 2022-06-08

Class II · Ongoing

Class II FDA medical device recall by GE Healthcare, LLC, initiated 2022-06-08. It names one FDA 510(k) clearance: K131977. Product: GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data within a computer network or on a workstation.. Reason: Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP).

Recalling firm: GE Healthcare, LLC
Classification: Class II
Status: Ongoing
Initiated: 2022-06-08
Firm location: Waukesha, WI, United States

510(k) clearances named in this recall

1 on FDA's record

K131977 — CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENTGE Healthcare·cleared 2013-09-17

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data within a computer network or on a workstation.

Reason for recall

Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)

Data sourced from openFDA. This site is unofficial and independent of the FDA.