FDA Medical devices recall ·
Core Services Hub V8, a set of backend services including Cross Enterprise… recall
- Recall number
- Z-3171-2026
- Date
- (initiated July 31, 2026)
- Company / brand
- GE Healthcare
500 W Monroe St, Chicago, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 250 systems
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it 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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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 SHOREMEMO25249340 VT27062091 NNAR25264207 107500-1-CoreServices Hub-27003899 UNIVERSITY26715185 MSI25263844 RRA24845093 RICHMONDU26628093 MFCI24810480 MFCI24825168 LMH25269182 TIET24966115 UTMC25263843 USOK26760295 CCA26850726 WYMH26492340 EVCH24849763 106483-1-Tenant CoreServices Hub-27124492 UHS125299932 ANMEDHEA25206013 ANMEDHEA26129703 CH1126596219TPCSHP CNOS26980316 OPP25269183 MHHS24845097 GZMG24848821 26885370TenantCSH 26898047StgTenCSH OVRLK25074987 Prod WFC 2 Prod WFC 1 EVG26454426 EVG26973916 M
Distribution
Worldwide - US Nationwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-3171-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.