GE Healthcare recalls

GE Healthcare has 518 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 23 Sep 2026. 144 are still ongoing. 9 were reported in the last 12 months.

Total recalls518since 2012
Last 12 months9reported
Class I357% of total
Ongoing144latest 23 Sep 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 35 7%Class II 477 92%Class III 6 1%

By year

Ongoing ge healthcare recalls

144 active

All ge healthcare recalls, newest first

518 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIEnterprise Archive V8 recalled by GE HealthcareGE HealthcareDevice MalfunctionNationwide
DeviceCLASS IIWorkflow Core Services V8, intended to provide set recalledGE HealthcareOtherNationwide
DeviceCLASS IICore Services Hub V8, a set of backend services including recalledGE HealthcareOtherNationwide
DeviceCLASS IICentricity Enterprise Archive V2, V3, and V4 recalled by GE HealthcareGE HealthcareDevice MalfunctionNationwide
DeviceCLASS IICentricity PACS V2, V3, V4, V6, V7 recalled by GE HealthcareGE HealthcareDevice MalfunctionNationwide
DeviceCLASS IICentricity PACS Server V7, intended recalled by GE HealthcareGE HealthcareOtherNationwide
DeviceCLASS IISigna Premier systems recalled by GE HealthcareGE HealthcareOtherNationwide
DeviceCLASS IICentricity Universal Viewer Zero Footprint Client recalledGE HealthcareDevice MalfunctionNationwide
DeviceCLASS IIGE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological recalledGE HealthcareDevice Malfunction
DeviceCLASS IICentricity Pacs-iw (Pacs-iw) recalled by GE HealthcareGE HealthcareOtherIL
DeviceCLASS IICentricity Pacs-iw with Universal Viewer recalled by GE HealthcareGE HealthcareOtherIL
DeviceCLASS IICentricity Universal Viewer Zero Footprint recalled by GE HealthcareGE HealthcareOtherNationwide
DeviceCLASS IICentricty PACS, V2, V3, V4, V6, V7 recalled by GE HealthcareGE HealthcareOtherIL
DeviceCLASS IIViewPoint; system, imaging processing, radiological recalledGE HealthcareOtherNationwide
DeviceCLASS IICentricity Universal Viewer Zero Footprint Client recalledGE HealthcareOtherIL
DeviceCLASS IIViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA recalledGE HealthcareOtherNationwide
DeviceCLASS IICentricity Pacs-iw recalled by GE HealthcareGE HealthcareDevice MalfunctionIL
DeviceCLASS IICentricity Universal Viewer Workflow Manager recalled by GE HealthcareGE HealthcareOtherNationwide
DeviceCLASS IICentricity Universal Viewer recalled by GE HealthcareGE HealthcareDevice MalfunctionIL
DeviceCLASS IIUniversal Viewer Workflow Manager recalled by GE HealthcareGE HealthcareOtherNationwide
DeviceCLASS IICentricity Pacs-iw with Universal Viewer recalled by GE HealthcareGE HealthcareOtherIL
DeviceCLASS IICentricity Pacs-iw, Product ID Numbers: a) recalled by GE HealthcareGE HealthcareOtherIL
DeviceCLASS IICentricity Universal Viewer, Centricity Universal Viewer recalledGE HealthcareOtherIL
DeviceCLASS IICentricity Pacs-iw with Universal Viewer recalled by GE HealthcareGE HealthcareOtherIL
DeviceCLASS IIGE Centricity Universal Viewer recalled by GE HealthcareGE HealthcareLabeling Errors40 states
DeviceCLASS IIService manuals for the CT, PET, or NM table as follows recalledGE HealthcareOtherNationwide
DeviceCLASS IICentricity PACS recalled by GE HealthcareGE HealthcareDevice MalfunctionNationwide
DeviceCLASS IIAvance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009 recalledGE HealthcareDevice Malfunction28 states
DeviceCLASS IAisys CS2 Anesthesia System recalled by GE HealthcareGE HealthcareOtherNationwide
DeviceCLASS IISigna Premier magnetic resonance scanner recalled by GE HealthcareGE HealthcareOtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.