ProductGuru Recalls

Official recall record

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model/Catalog/Code Numbers: a)¿¿¿¿¿ 2089507-120; b)¿¿¿¿ 2089507-129;

US FDA — Medical Devices · 2024-08-29 · United StatesClass II
Issuing authority
US FDA — Medical Devices
Alert date
2024-08-29
Country of alert
United States
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
840682102988
Brand on record
GE Healthcare

What the authority reported

GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) version v6.0 SP11.x where the latest report is not shown by default to the user. The issue may occur when a study has multiple DICOM structured reports (i.e. preliminary, final, and/or addendum) stored in different series.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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