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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 Centricity Universal Viewer Recalled for Potential Patient Mismatch

Agency Publication Date: February 27, 2026
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Summary

GE Healthcare has recalled approximately 250 units of the Centricity Universal Viewer Zero Footprint Client (ZFP) software versions SP11.6, SP11.6.0.1, and SP11.6.1. Under certain workflows on systems with Patient Timeline installed, the viewer may display clinical images that do not match the patient information shown on the screen. Consumers should contact GE Healthcare or their system administrator to arrange for a software correction or update.

Risk

The software defect can cause a healthcare provider to view one patient's radiological images while the screen displays a different patient's name and data. This mismatch could lead to incorrect diagnoses or improper medical treatment based on the wrong patient's imaging results.

What You Should Do

  1. Identify if your facility is using Centricity Universal Viewer Zero Footprint Client versions ZFP v6.0: SP11.6, SP11.6.0.1, or SP11.6.1 with Patient Timeline installed.
  2. Check your system ID or model numbers (2110344-039, 2110344-046, or 2110344-047) against the affected list. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device immediately to prevent patient data mismatches.
  4. Contact GE Healthcare or your system distributor to arrange for a software repair, replacement, or correction.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls for additional questions.

Your Remedy Options

๐Ÿ“‹Other Action

Software correction or update.

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: GE Healthcare Centricity Universal Viewer Zero Footprint Client
Variants: ZFP v6.0: SP11.6, ZFP v6.0: SP11.6.0.1, ZFP v6.0: SP11.6.1
Model / REF:
2110344-039
2110344-046
2110344-047
Serial Numbers (250):
105906-2-Centricity Universal Viewer Zero Footprint / ZFP-02312614
4491-1-Centricity Universal Viewer Zero Footprint / ZFP-22180897
10908-1-Centricity Universal Viewer Zero Footprint / ZFP-25199248
10908-7-Centricity Universal Viewer Zero Footprint / ZFP-22203146
10908-7-Centricity Universal Viewer Zero Footprint / ZFP-25188736
4263-3-Centricity Universal Viewer Zero Footprint / ZFP-00106869
4263-3-Centricity Universal Viewer Zero Footprint / ZFP-00106870
4263-5-Centricity Universal Viewer Zero Footprint / ZFP-01300798
3064-15-Centricity Universal Viewer Zero Footprint / ZFP-25222931
3064-15-Centricity Universal Viewer Zero Footprint / ZFP-25248683
3064-15-Centricity Universal Viewer Zero Footprint / ZFP-25248688
3064-15-Centricity Universal Viewer Zero Footprint / ZFP-25248690
3064-15-Centricity Universal Viewer Zero Footprint / ZFP-25248695
3064-15-Centricity Universal Viewer Zero Footprint / ZFP-25248713
3064-15-Centricity Universal Viewer Zero Footprint / ZFP-25248716
3064-15-Centricity Universal Viewer Zero Footprint / ZFP-26608643
10458-9-Centricity Universal Viewer Zero Footprint / ZFP-26580437
10458-9-Centricity Universal Viewer Zero Footprint / ZFP-26694204
10458-9-Centricity Universal Viewer Zero Footprint / ZFP-26694229
105197-2-Centricity Universal Viewer Zero Footprint / ZFP-20813950
4642-6-Centricity Universal Viewer Zero Footprint / ZFP-25210052
4642-6-Centricity Universal Viewer Zero Footprint / ZFP-25210057
4642-6-Centricity Universal Viewer Zero Footprint / ZFP-25210107
103829-6-Centricity Universal Viewer Zero Footprint / ZFP-20900298
103829-6-Centricity Universal Viewer Zero Footprint / ZFP-21180523
103829-6-Centricity Universal Viewer Zero Footprint / ZFP-21180525
3212-5-Centricity Universal Viewer Zero Footprint / ZFP-26390526
3212-5-Centricity Universal Viewer Zero Footprint / ZFP-26694221
3212-5-Centricity Universal Viewer Zero Footprint / ZFP-26694222
10360-3-Centricity Universal Viewer Zero Footprint / ZFP-24463042
10360-3-Centricity Universal Viewer Zero Footprint / ZFP-25239139
10360-3-Centricity Universal Viewer Zero Footprint / ZFP-25239140
10360-3-Centricity Universal Viewer Zero Footprint / ZFP-26714200
10360-3-Centricity Universal Viewer Zero Footprint / ZFP-26714202
3471-36-Centricity Universal Viewer Zero Footprint / ZFP-24399434
3471-36-Centricity Universal Viewer Zero Footprint / ZFP-26295812
1198-18-Centricity Universal Viewer Zero Footprint / ZFP-02348419
1198-18-Centricity Universal Viewer Zero Footprint / ZFP-18990433
1198-78-Centricity Universal Viewer Zero Footprint / ZFP-22223452
100581-1-Centricity Universal Viewer Zero Footprint / ZFP-25168130
8746-1-Centricity Universal Viewer Zero Footprint / ZFP-23900206
8746-1-Centricity Universal Viewer Zero Footprint / ZFP-21318104
1207-14-Centricity Universal Viewer Zero Footprint / ZFP-24836084
2123-19-Centricity Universal Viewer Zero Footprint / ZFP-24836053
102901-1-Centricity Universal Viewer Zero Footprint / ZFP-23251238
3922-17-Centricity Universal Viewer Zero Footprint / ZFP-00098229
3922-18-Centricity Universal Viewer Zero Footprint / ZFP-24466083
3922-18-Centricity Universal Viewer Zero Footprint / ZFP-26132903
3922-18-Centricity Universal Viewer Zero Footprint / ZFP-26132895
3922-18-Centricity Universal Viewer Zero Footprint / ZFP-24466076
UDI:
00840682102988

Affected units are specifically those on systems with Patient Timeline installed.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98368
Status: Active
Manufacturer: GE Healthcare
Sold By: Authorized GE Healthcare distributors; Direct B2B healthcare facility sales
Manufactured In: United States
Units Affected: 250 units
Distributed To: Nationwide

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.

Find an Attorney

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.