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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

GE Medical Systems, LLC: There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

Agency Publication Date: March 16, 2026
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Summary

GE Medical Systems, LLC is recalling approximately 2,405 units of Centricity Universal Viewer software, including various versions from 5.0 through 7.0. The software, used to display medical images and mammograms, has a cybersecurity flaw where user login passwords could be exposed on local workstations. If you use this software in a healthcare setting, please contact your healthcare provider or the manufacturer for security patches and guidance.

Risk

An unauthorized individual could use exposed login credentials to access the system, which may allow them to manipulate sensitive medical data or disrupt the availability of the imaging system. While the potential for data manipulation exists, no specific incidents or injuries have been reported to date.

What You Should Do

  1. Identify if your facility is using Centricity Universal Viewer Software Versions 5.0 SP6 through 5.0 SP7.1, Versions 6.0 through 6.0 Sp10.4.1, or Versions 7.0 through 7.0 Sp2.0.1.
  2. Check for specific Model Numbers and Product IDs, such as model numbers 5826659-027, 2088026-406, or 2088026-026, which are associated with this security notice.
  3. Immediately contact your local GE Medical Systems service representative or healthcare provider to receive information regarding cybersecurity patches or software updates to mitigate this vulnerability.
  4. Monitor your imaging systems for any unauthorized access or unusual data activity until the system has been secured.
  5. Contact the FDA at 1-888-463-6332 if you have additional questions or wish to report a software issue.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer initiated cybersecurity vulnerability mitigation.

How to: Contact your healthcare provider or the manufacturer for further instructions and potential patch availability.

Affected Products

Product: Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1
Model / REF:
5826659-027
5826659-029
5826659-032
5826659-033
5826659-028
5826659-034
5826659-030
5826659-019
5826659-022
5826659-026
5826659-023
5826659-031
5826659-025
5826659-002
5826659-021
5826659-037
5826659-014
5826659-016
5826659-013
UPC Codes:
00840682145794
Product: Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1
Model / REF:
2088026-406
2100169-001
2088026-985
2088026-971
2088026-614
2088026-713
2088026-994
2100491-006
2088026-723
2088026-308
2104867-044
2100491-012
2088026-962
2088026-969
2102676-001
2088026-936
2088026-960
K1220JWED
2088026-806
2088026-506
2088026-026
2088026-970
2088026-943
2088026-990
2088
UPC Codes:
00840682103800
Product: Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1
Model / REF:
2088026-026
2088026-115
2088026-043
K2042VJED
2088026-132
2088026-003
2088026-110
2089629-003
2066908-136
2066908-150
Lot Numbers:
4446-2-Centricity Universal Viewer-00558643
100256-3-Centricity Universal Viewer-00558700
101044-1-Centricity Universal Viewer-00558694
13240-2-Centricity Universal Viewer-00558103
4441-1-Centricity Universal Viewer-00558677
4578-1-Centricity Universal Viewer-00558340
10831-2-Centricity Universal Viewer-00558682
656341-Centricity Universal Viewer-01431499
50567-Centricity Universal Viewer-02176369
2690973-Centricity Universal Viewer-01454622

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98428
Status: Active
Manufacturer: GE Medical Systems, LLC
Manufactured In: United States
Units Affected: 3 products (1568 units; 797 units; 40 units)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.