Recall Z-3167-2026

GE Healthcare · initiated July 31, 2026

Open, Classified

Product

Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions

Codes / lots: UDI-DI: V4 - 00195278409287; System IDs: BIRMINGHAM20886386 SevierCou21180101 SevierCou21180111 UOAR24851211 UOAR23214501 CARTI27326017 KGM21766613T KGM21332085 KGM21677289 HRH323169307 HONORHEALT21179400 MIHS25042933 MIHS25151161 MIHS25042933 MIHS25151165 MIHS25151166 ADHR27301883 PMIO26874972 PMHD27236488 PIPELINEH26974662 PIPELINEH27011598 SANFERNAN23238694 KRM22180898 MHL23269965 SUTH26668887 NORV21741298 24931893EdgeEA 25083358StgEdgeEA VCM27268846 SCRL24283967 SCRL23202147 SFGH24285530 USHC25292971 USHC26580362 GSH321314340 LosRobles23253832 QTHBL26325570 DENVERVA21733821 DENVER VA24406115 BOULDER22107026 BOULDER22107318 BOULDERCO24954910 HHL27121414 Not Available GRHD20869082A GRHD20869563B GRHD20870041T GRHD27231932 Not Available VVMC21290279 VVMC24397815 VVMC23203058 DDOC26923413 BAYHEALTH22212474 BAYHEALTH23201150 BAYHEALTHxxx BAYHEALTH26871762 JFKR20875123CEAGW 100029-1-Enterprise Archive-27124494 106428-3-Enterprise Archive-21313581 BYH24954908 BYH26856929 BYH26856932 LMC421600077 MH820838229 BIHT21020972 BIHT21305845 BIHT21305846 BIHT21305854 BIHT21305855 BIHT21305856 BIHT21310361 MH826770189 KRMC22464526 KRMC23157942 OFMC22161730T OFMC23066623P ORDC20944523…

Reason for recall

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.

FDA-determined cause: Under Investigation by firm

Action taken

An URGENT MEDICAL DEVICE CORRECTION notification letter dated 7/31/26 was sent to customers. Actions to be taken by Customer/User Pending corrections from GE HealthCare, you can continue to use your systems by following the instructions below. 1. Do not perform any new inbound data (DICOM) migration projects. Please contact GE HealthCare before starting any new migration projects. 2. If using Enterprise Archive with Core Services Hub/Workflow Core Services, when reviewing or exporting prior imaging studies after migration to Enterprise Archive, verify that the study and images within the study are associated with the correct patient as follows: At the Study level: " Compare name, date of birth, and patient identifiers only if burned-in or embedded in the image. Do not rely on patient information in the image overlays that can be toggled on and off. " If burned-in or embedded patient identifiers are not available, compare with prior studies based on patient anatomy, implants, or unique anatomical features. At the Image level: " Confirm that the images within the study do not belong to different patients based on acquisition date and time or other patient identifiers. Please maintain any previous source systems or migration servers pending correction of this issue by GE HealthCare. Please ensure that all potential users in your facility are made aware of this safety notification and the recommended actions above. Please retain this document for your records. Please complete and return the attached acknowledgement form electronically via FMI 85492 Digital Response Form or print, fill out manually, scan, and email to recall.85492@gehealthcare.com. If you have any questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or your local Service Representative.

Details

Recall number
Z-3167-2026
Initiated
July 31, 2026
Posted by FDA
September 15, 2026
Product code
LLZ – System, Image Processing, Radiological
Quantity
1298 systems
Distribution
Worldwide - US Nationwide distribution.
Recalling firm
GE Healthcare, Chicago, IL

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-3166-2026 Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving…Under certain conditions historical imaging data migrated from a legacy system may become incorrectly… 07/31/2026Open, Classified
Z-3168-2026 Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage…Under certain conditions historical imaging data migrated from a legacy system may become incorrectly… 07/31/2026Open, Classified
Z-3169-2026 Centricity PACS Server V7, intended for managing digital medical images and associated…Under certain conditions historical imaging data migrated from a legacy system may become incorrectly… 07/31/2026Open, Classified
Z-3170-2026 Workflow Core Services V8, intended to provide set of services for storage and retrieval…Under certain conditions historical imaging data migrated from a legacy system may become incorrectly… 07/31/2026Open, Classified
Z-3171-2026 Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and…Under certain conditions historical imaging data migrated from a legacy system may become incorrectly… 07/31/2026Open, Classified