FDA Device recall Z-3171-2026
Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise im…
- FDA Device
- Class II
- ongoing
- Published 2026-09-23
On 2026-09-23 the FDA classified a Class II recall of Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise im… by Ge Healthcare, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3171-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-31 |
| Published | 2026-09-23 |
| Last updated | 2026-09-29 05:30 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise imaging workflows, All versions
Reason
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.
Identifiers
| code_info | System IDs: CARTI27326018 KGM24849767P2 KGM26790380P1 KGM26790386T1 KGM26790388T2 PIPELINEH26974665 PIPELINEH27036913 K…System IDs: CARTI27326018 KGM24849767P2 KGM26790380P1 KGM26790386T1 KGM26790388T2 PIPELINEH26974665 PIPELINEH27036913 KRM25208408 26885371TenantCSH 26897935StgTenCSH VVMC25199249 Not Available VVMC26130320 DDOC26923416 BAYHEALTH26580398 BAYHEALTH26871765 JFKR27127669 LAKESIDEM27124493 BYH25222926 LMC427127671 KRMC27127670 MH826900861 ICA27062095 NORTHWEST24866978-XE NORTHWEST27294841-XE NORTHWEST27294843-XE JHSJHOCC24849766 ANN & ROBE24866975 JHSJHOCC27005469 GOSH26799709CSHP GOSH26848483CSHT CMAE26304473 CMAE26774289 MSUHEALTH26980323 Not Available CHILDRENS24808132 XE VCP 103829-6-CoreServices Hub-XE VMP 103829-6-CoreServices Hub-XE Test 103829-6-CoreServices Hub-WFC VCP 103829-6-CoreServices Hub-WFC VMP 103829-6-CoreServices Hub-WFC Test OMCR25206023 ETP Prod CoreServices 1 ETP Prod CSH 2 CHILDRENS25171538 26885369TenantCSH BC325168126 BC324829461 BC325239077 BC325239084 BC326538517 NCDC26959094 MINNETOHE26945472 AMIM27062090 VTH26323581 SHOREMEMO24810482 SHOREMEMO24988230 SHOREMEMO |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-29 05:30 UTC. Current status: ongoing.
Other recalls by Ge Healthcare
- Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation, distrib…
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Adminis…
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions
FDA Device · Class II · 2026-09-23 · Ge Healthcare
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3171-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.