FDAJuly 15, 2022device

(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX; (3) GE Universal Viewer 8.0, Model 5865740-00x.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Inaccurate Distance and Area measurements with use of Global Stack viewport.

What to do

FDA enforcement status: Ongoing

Brands named

ge healthcare

UPCs

00840682103800008406821457940084068214555800195278379610

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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