FDA recall, , Moderate risk
GE Healthcare Centricity Universal Viewer Zero Footprint Client
The viewer may show patient information that does not match the images displayed.
Summary by Recall Canary from the FDA notice
What happened
GE Healthcare is recalling its Centricity Universal Viewer Zero Footprint Client because, under certain workflows, patient information shown in the viewer may not match the images displayed. The recall, which the company began on January 16, 2026, was added to the FDA's Enforcement Report on February 27, 2026, and covers 250 units distributed worldwide, including the US Nationwide and countries such as Canada, Germany, Japan, and the United Kingdom.
The affected versions are ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed. The product is described as a System, Image Processing, Radiological. The recall was classified by the FDA on February 27, 2026, and listed in the FDA's weekly enforcement report on March 11, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number, UDI-DI and other code are listed under that product.
A UDI-DI is the device identifier printed with the barcode on the device label.
GE Healthcare Centricity Universal Viewer Zero Footprint Client
- Model number
- 2110344-039
- 2110344-046
- 2110344-047
- UDI-DI
- 00840682102988
- Other code
- 02312614
- 22180897
- 25199248
- 22203146
- 25188736
- 00106869
- 00106870
- 01300798
- 25222931
- 25248683
- 25248688
- 25248690
- 25248695
- 25248713
- 25248716
- 26608643
- 26580437
- 26694204
- 26694229
- 20813950
- 25210052
- 25210057
- 25210107
- 20900298
- 21180523
- 21180525
- 26390526
- 26694221
- 26694222
- 24463042
- 25239139
- 25239140
- 26714200
- 26714202
- 24399434
- 26295812
- 02348419
- 18990433
- 22223452
- 25168130
- 23900206
- 21318104
- 24836084
- 24836053
- 23251238
- 00098229
- 24466083
- 26132903
- 26132895
- 24466076
All 271
- 24466077
- 24466078
- 24466079
- 24466088
- 00098228
- 20098431
- 20036715
- 25014571
- 24480189
- 22206970
- 26356112
- 25151288
- 26548614
- 20569855
- 20575531
- 20575532
- 20575543
- 20575533
- 20575535
- 02283242
- 02170574
- 01819807
- 01225123
- 01225124
- 21180575
- 21200874
- 01265320
- 01265321
- 01265322
- 21200873
- 01265323
- 01225125
- 01265343
- 21207211
- 26379461
- 21214076
- 26617853
- 00044391
- 00117236
- 00117239
- 02394845
- 16921400
- 25194303
- 26608620
- 19670323
- 01286629
- 26660354
- 00163499
- 00260806
- 01461578
- 22186138
- 26703904
- 26703931
- 26703990
- 24944069
- 26859675
- 24467504
- 02286748
- 26624821
- 26624822
- 26624823
- 26624824
- 26624826
- 26624828
- 26624829
- 26304641
- 22169581
- 25287444
- 26748573
- 20108177
- 22203508
- 24336091
- 26608610
- 25017402
- 00001140
- 26666351
- 26666352
- 26666354
- 26666356
- 26599556
- 12711614
- 26449902
- 25304950
- 25329396
- 21198479
- 01271448
- 25204625
- 16872968
- 24855625
- 26929832
- 11388609
- 24448019
- 26640843
- 16999320
- 24833747
- 24434112
- 24439350
- 25203487
- 26906289
- 24838806
- 24305476
- 26127359
- 20978978
- 20587825
- 24931880
- 26136995
- 26917029
- 26917028
- 01819295
- 17026623
- 25248193
- 24525506
- 17191257
- 26628542
- 17066964
- 24484202
- 25169256
- 16951628
- 26453548
- 25227096
- 00066573
- 22879437
- 24281567
- 17111683
- 21733830
- 25194300
- 17021465
- 24487930
- 25210479
- 24465830
- 26802528
- 19666476
- 24846063
- 20618153
- 24821472
- 20997395
- 00038193
- 0853550198
- 02093675
- 00116181
- 00158571
- 25022095
- 00555894
- 26560468
- 00165095
- 21322536
- 26631095
- 25309376
- 26784611
- 17053632
- 24829942
- 24825373
- 17152365
- 26632357
- 17040488
- 26404455
- 26923415
- 26898336
- 22180910
- 22180906
- 26705438
- 26839308
- 26839310
- 26839311
- 26839312
- 26839313
- 26715184
- 26850722
- 26747422
- 21237479
- 26884848
- 26884853
- 17094888
- 26918064
- 26747414
- 26769258
- 26769261
- 24388499
- 21350494
- 24388493
- 24388494
- 24388495
- 24388497
- 24388498
- 24388490
- 24388491
- 24388492
- 24484469
- 24374380
- 21359919
- 26865306
- 26671908
- 26689509
- 02360544
- 26918260
- 23297397
- 26880666
- 17195358
- 23986377
- 26799525
- 26800953
- 17121345
- 26796880
- 17775055
- 26880655
- 26912759
- 26824375
- 26805562
- 16959088
- 26777223
- 26368616
- 26825072
- 26876144
- 16882165
- 26673881
- 16880927
- 26818090
- 22138067
- 22138066
- 25012607
- 24475044
Recall details
- Company began the recall
- Sold in
Worldwide distribution - US Nationwide and the countries of Belarus, Brazil, Canada, China, France, Georgia, Germany, India, Indonesia, Ireland, Israel, Italy, Japan, Korea (Republic Of), Kuwait, Lebanon, Malaysia, Netherlands, Philippines, Poland, Russia, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkiye, United Arab Emirates, United Kingdom, Vietnam.
- Company
- GE HealthcareChicago, Illinois
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98368
- Recall number
- Z-1475-2026
- Quantity recalled
- 250 units
All recalls from GE Healthcare
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
