CLASS II ONGOING Device recall · Reported 23 Sep 2026 · FDA Enforcement Report
Workflow Core Services V8, intended to provide set recalled
GE Healthcare is recalling Workflow Core Services V8, intended to provide set of services for storage and retrieval, distributed nationwide in the US. The recall was initiated on 31 Jul 2026 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-3170-2026
- FDA event ID
- 99661
- Recalling firm
- GE Healthcare, Chicago, IL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 31 Jul 2026
- FDA classified
- 15 Sep 2026
- Reported
- 23 Sep 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 31 Jul 2026 | Recall initiated by company | |
| 15 Sep 2026 | Classified by FDA | +46 days |
| 23 Sep 2026 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Product as listed by the FDA
Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administration, common configuration management for consuming applications, All versions
Where it was distributed
Worldwide - US Nationwide distribution.
Questions about this recall
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.
Which lots are affected?
System IDs: SevierCou21180109 PMIO26874968 VCM27268845 QTHBL25025522 GRHD20869086A GRHD20869566B GRHD20870043T VVMC22203148 LAKESIDEM22311789 OFMC22161726 OFMCProd24283369 AMCL20962675 LAKESIDEM21200035 NEUROSKEL22629460 FLMC24849713 FLMC23269955 MRMC220924399 MRMC221300628 MRMC221300631T 106684-1-Workflow Core Services-23253822 MRMC221306901 LaitekDataMigrationETPLab1WFC LaitekDataMigrationETPLab2WFC CMCM24346488 QTHDD22236119 QTHDD24934127 24489144TruePACSWFC 25248966TruePACSWFCT 22144965True_PACSWFC HANN21755240 HRHWFC HANN24283725 BC324463044 AMIM27024664 CHERRYCOU20906543 CHERRYCOU21180589T REDI21237465 MDHC26580426 VT25202652 NNAR21175649 104680-1-Workflow Core Services-24492064 NYK20996006 NYK21803243 NYK21803244 UNIVERSITY20575614 26325561TenantWFC NEWYORK26794149 26932125StgTenWFC 26403778TenantWFC RICHMONDU23210868 RICHMONDUWFCTest MFCI25178603 HZC20924408 HZC23291365 106633-1-Workflow Core Services-22208526 CCA20533413 CCA20609478 EVCH22176263 VBHC25014585 27109610TenantWFC 27112412StgTenWFC CMSImagingWFC HRMC21704042 Not Available 106520-1-Workflow Core Services-21291109 OPP25014573 DRISCOLLC26738355 MCHD120544438 MCHD20609496 URSA20991949 GZMG24480191 24819548TenantWFC EVG22631301 25199257TenantWFC Not Available Not Available Not Available Not Available Test TP PROD TP Not Available Not Available Test TP Prod TP Not Available Not Available 672721-Workflow Core Services-24280401 313741-Workflow Core Services-24280410 Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available Not Available 24488449 24488458 Not Available Not Available TBD Not Available tbd Not Available Not Available Not Available Not Available Not Available Not Available 106738-1-Workflow Core Services-24437872 HKBH21752373 534530-Workflow Core Services-23217329 SP_FORT_ETP_WFC RAPTAKOS_WFC_1 MMHRC-WFC RSUripSumoharjo_WFC PTAFFINITYHEALTH_WFC BETHSAIDA-ETP-WFC KeluargaGrandWisata-ETP-WFC RSUnpadJatinangor_WFC TestWFCKafeel01 Not Available Not Available 22138578 22138587 26991270 Not Available 24268633 Not Available 24336871 24336879 26978075 27079476 22225245 Not Available Not Available Not Available Not Available Not Available Not Available MOH-MY-WFC INTEGRATEDONCOLOGY-WFC Not Available Not Available ROP_TEMP002 MariaReyna-XavierUH-WFC StPaulHospital-WFC CMHCP27015653 Inobe23986382 PL3362-Workflow Core Services-22820442 SA1411_WFC SA1196_WFC 26368629 WFC_ETPACS_GON5361362 Not Available SrisawanBH-WFC 16861859 - WFC 16861859 - WFC2 ROH24368412P PRECISIONMEDICAL-WFC
Where was it sold?
Worldwide - US Nationwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 29 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
5 other products · FDA event 99661This product is part of a recall event; the main page for the event is Centricity PACS Server V7, intended recalled by GE Healthcare.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Centricity PACS Server V7, intended recalled by GE Healthcare | GE Healthcare | Other | Nationwide | |
| CLASS II | Centricity PACS V2, V3, V4, V6, V7 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide | |
| CLASS II | Centricity Enterprise Archive V2, V3, and V4 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide | |
| CLASS II | Core Services Hub V8, a set of backend services including recalled | GE Healthcare | Other | Nationwide | |
| CLASS II | Enterprise Archive V8 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide |
More recalls from GE Healthcare
All 518| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Enterprise Archive V8 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Core Services Hub V8, a set of backend services including recalled | GE Healthcare | Other | Nationwide |
| Device | CLASS II | Centricity Enterprise Archive V2, V3, and V4 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Centricity PACS V2, V3, V4, V6, V7 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Centricity PACS Server V7, intended recalled by GE Healthcare | GE Healthcare | Other | Nationwide |
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