CLASS II ONGOING Device recall · Reported 13 Jul 2022 · FDA Enforcement Report

GE Centricity Universal Viewer Zero Footprint recalled by GE Healthcare

GE Healthcare is recalling GE Centricity Universal Viewer Zero Footprint. The recall was initiated on 8 Jun 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI 00840682102988, Versions 6.0 SP6 through SP11.4

Quantity recalled1,934 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1333-2022
FDA event ID: 90454
Recalling firm: GE Healthcare, Waukesha, WI
Classification: Class II
Status: Ongoing
Recall initiated: 8 Jun 2022
FDA classified: 5 Jul 2022
Reported: 13 Jul 2022
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Labeling Errors
Device type: Other Medical Devices

Timeline

8 Jun 2022	Recall initiated by company
5 Jul 2022	Classified by FDA	+27 days
13 Jul 2022	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

Worldwide distribution.

Questions about this recall

Is GE Centricity Universal Viewer Zero Footprint recalled?

Yes. GE Healthcare recalled GE Centricity Universal Viewer Zero Footprint on 8 Jun 2022. The recall is Class II and its status is Ongoing. Recall number Z-1333-2022.

Why was it recalled?

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

Which lots are affected?

UDI 00840682102988, Versions 6.0 SP6 through SP11.4

Where was it sold?

Worldwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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