Reported May 10, 2023 · Ongoing

Centricity PACS-IW with Universal Viewer, Model/Catalog Numbers: a) 2066908-061, b) 2066908-077, c) 2066908-086, d)…

GE Healthcare

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 · 500 W Monroe St · Chicago, IL · 60661-3671

Is this the product you have?

  • Centricity PACS-IW with Universal Viewer
  • Model/Catalog Numbers
    • a) 2066908-061
    • b) 2066908-077
    • c) 2066908-086
    • d) 2066908-111
    • e) 2066908-123
    • f) 2066908-136
    • g) 2066908-150
    • Radiological Image Processing System
Lot codes and dates

7 of 7 products

Products covered by this recall
#Product as published
12066908-061, Product ID Numbers: HC3062-Centricity Universal Viewer-01462397
22066908-077, Product ID Numbers: YP3150-Centricity Universal Viewer-01639018
32066908-086, Product ID Numbers: 100707-1-Centricity Universal Viewer-00558649, 9842-4-Centricity Universal Viewer-19386293
42066908-111, Product ID Numbers: 1045-1-Centricity Universal Viewer-00558651, 1045-1-Centricity Universal Viewer-19607785
52066908-123, Product ID Numbers: 4705-1-Centricity Universal Viewer-02398923
62066908-136, Product ID Numbers: 4723-1-Centricity Universal Viewer-02303576, 104648-2-Centricity Universal Viewer-02354806, 101272-1-Centricity Universal Viewer-00558671, ZA2533-Centricity Universal Viewer-00116577, 280801-Centricity Universal Viewer-19737221
72066908-150, Product ID Numbers: 100759-1-Centricity Universal Viewer-02360986, 100713-1-Centricity Universal Viewer-00558259, 100713-1-Centricity Universal Viewer-01982629, 100512-1-Centricity Universal Viewer-00558264, 3727-1-Centricity Universal Viewer-00558421, RU9761-UW PACS-IW UP TO 10K-02336112
Amount recalled
17 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Why it was recalled

GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:34 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.