Reported Oct 24, 2018 · Terminated

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

GE Healthcare, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Healthcare, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.
Lot codes and dates
  • SYSTEM ID315470CPUWPV UDI #: 8406821038 00DE #: 2090255-001
Amount recalled
1

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 31, 2022 · Data as of Sep 19, 5:31 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.