Every recall we track for GE Healthcare — 22 in all — plus the complaints and injury reports the public filed about them.
GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client models 2110344-039, 2110344-046, 2110344-047 due to potential patient information mismatch in certain workflows with specific software versions.
GE Healthcare recalls Centricity Universal Viewer (UV) models with potential security vulnerability allowing unauthorized access to patient data. Affected models include 2066908-077, 2066908-136, 2066908-150, and others. No remedy specified in recall.
GE Healthcare recalls Centricity Cardiology CA1000 devices with specific model numbers due to a potential security vulnerability that could allow unauthorized access to patient data.
GE Healthcare recalls specific Centricity PACS-IW models due to potential security vulnerability allowing unauthorized access to patient data. Affected units include models 2042988-001 and 2049587-009 through 2049587-015.
GE Healthcare recalls Centricity Radiology RA600 systems with specific model numbers due to a security vulnerability that could allow unauthorized access to patient data. Affected units include models 2022296-001, 2033901-001, and others listed in the recall notice.
GE Healthcare recalls specific Centricity PACS-IW models with Universal Viewer due to potential security vulnerability allowing unauthorized access to patient data. Affected units may need updates to prevent data breaches.
GE Healthcare recalls Centricity Universal Viewer Zero Footprint devices with specific model numbers due to a potential security vulnerability that could allow unauthorized access to patient data.
GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client v6.0 SP11.x where reports aren't shown by default when multiple DICOM structured reports exist in different series.
GE Healthcare recalls Centricity PACS V2, V3, V4, V6, V7 systems where image storage fails when reaching maximum unique identifiers, potentially causing partial study acquisitions. Affected units have specific UDI/DI codes listed in the recall.
GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client versions v6.0 SP9.x and SP10.x where addended reports aren't shown by default when created on the same day as original reports but at different times, in IE10, IE11, and Firefox.
GE Healthcare recalls Centricity PACS-IW software versions V3.7.x through 3.7.3.9 SP3 due to potential image mixing from two patients in a single study. Affected units include specific installation IDs listed in the recall notice.
GE Healthcare recalls Centricity Universal Viewer software versions 6.0 SP0 through 6.0 SP7.1 due to potential image mixing from two patients in a single study. Affected units include specific model numbers and installation IDs.
GE Healthcare recalls Centricity PACS-IW software versions with risk of mixing images from two patients in a single study. Affected units may need correction to prevent misdiagnosis.
GE Healthcare recalls Centricity Universal Viewer Workflow Manager software versions that may display incorrect patient information when launching exams via third-party applications.
GE Healthcare recalls Universal Viewer Workflow Manager software versions that may display incorrect patient information when launching exams via third-party applications. Affected units include specific software versions and product IDs.
GE Healthcare recalls specific Centricity PACS-IW models due to potential mismatch of patient information when correcting records. Affected units include product IDs starting with 2041037-001 through 2052829-001.
GE Healthcare recalls specific Centricity Universal Viewer models due to risk of mismatched patient information when correcting study details. Affected units include models with catalog numbers 2088026-003 through 2104867-045.
GE Healthcare recalls Centricity PACS-IW with Universal Viewer models that may mismatch patient data during corrections, risking incorrect medical records. Affected units include specific catalog numbers and product IDs.
GE Healthcare recalls OEC 9900 C-Arm fluoroscopy systems in the US that may not display required dose values per regulations. Affected units were configured to show AKR/CAK instead of DAP when leaving the factory.
GE Healthcare recalls Centricity PACS-IW systems with model numbers 2052831-00X and 2049588-008. A database error can cause images to be missing during exams, especially with very small image sets like a single CR Thorax image.
GE Healthcare recalls Centricity Universal Viewer devices that may display mammograms without warning if image series are missing from exams.
GE Healthcare recalls Centricity PACS-IW with Universal Viewer devices that may show missing medical images without warning, risking incorrect diagnoses. Affected units include specific model numbers listed in the recall notice.
