Reported Sep 23, 2026 · Ongoing
Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical…
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 Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions
- Lot codes and dates
24 of 24 products
Products covered by this recall Model / number Barcodes Product as published 082499180102082499190198082445110005082455060001 tbd 082499130790 082499130124 082499020074082499030205SiteID-Centricity Enterprise Archive-20608302 SiteID-Centricity Enterprise Archive-20608323 SiteID-Centricity Enterprise Archive-20608324 SiteID-Centricity Enterprise Archive-20608390 SiteID-Centricity Enterprise Archive-20608393 SiteID-Centricity Enterprise Archive-20608394 SiteID-Centricity Enterprise Archive-20608408 SiteID-Centricity Enterprise Archive-20608410082455040342SiteID-Centricity Enterprise Archive-20637766082455040321082499290047— 0824992900470824550400251359772-Centricity Enterprise Archive-21327383082421230658082499220115— 8245523001608245503007382455150068 82455150074 SiteID-Centricity Enterprise Archive-20608838082455180040082499180080— 082499060054082499100395SiteID-Centricity Enterprise Archive-20594649 SiteID-Centricity Enterprise Archive-20594650 SiteID-Centricity Enterprise Archive-20606492 SiteID-Centricity Enterprise Archive-20595019 SiteID-Centricity Enterprise Archive-20541554 647002-Centricity Enterprise Archive-22252504 82499100387082499100394SiteID-Centricity Enterprise Archive-20606493082433120225082455180042082455180041 SiteID-Centricity Enterprise Archive-20594360082455120545082499100188— 82455290014082421130135SiteID-Centricity Enterprise Archive-20611137 SiteID-Centricity Enterprise Archive-20611755 SH-CH-Centricity Enterprise Archive-20614728 82455130335 82455130055 82455130394 8245513022408249918008508245516003582455120514 SiteID-Centricity Enterprise Archive-20594353 82455120227 JS KUNSHAN 123253814 82455080025 SiteID-Centricity Enterprise Archive-20608412082421050162SiteID-Centricity Enterprise Archive-20608172 417238-Centricity Enterprise Archive-21273761082455050069tbd 082427150109 082455130415 082499310137082499130813082499130813— 082499130813082499130813082499130813— 08249913081308249913081113767625-Centricity Enterprise Archive-2127376608245508002782455120448 - Amount recalled
- 1856 systems
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.
This product could cause temporary or reversible health problems — stop using it.
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