Generic Name: General-purpose Diagnostic Imaging System Workstation Trade Name: Centricity Universal Viewer

Recalling firm

Name of manufacturer: GE Healthcare Japan K.K. Location of manufacturer: 4-7-127 Asahigaoka, Hino-shi, Tokyo Type of license: Type 1 medical device manufacturer license number: 13B1X00150...

Product

Lot: 製造番号 ： YP0040、YP0079、YP0085、YP0086、YP0087、YP0088、YP0091、YP0092、 YP0094、YP0095、YP0096、YP0100、YP0110、YP0112、YP0113、YP0114、 YP0115、YP0117、YP0118、YP0119、YP0120、YP0121、YP0123、YP0124、 YP0125、YP0126、YP0127、YP0128、YP0129、YP0130、YP0131、YP0132、 YP0133、YP0134、YP0135、YP0136、YP0137、YP0138、YP0139、YP0141、 YP0142、YP0144、YP0145、YP0146、YP0147、YP0148、YP0149、YP0150、 YP0151、YP0152、YP0153、YP0154、YP0155、YP0157、YP0158、YP0159、 YP0160、YP0161、YP0162、YP0163、YP0164、YP0165、YP0166、YP0167、 YP0168、YP0169、YP0170、YP0171、YP0172、YP0173、YP0174、YP0175、 YP0176、YP0177、YP0178、YP0179、YP0180、YP0181、YP0182、YP0183、...

Reason

The manufacturer has reported the existence of a security vulnerability in devices equipped with certain software versions (5.0 SP6-5.0 SP7.1, 6.0-6.0 SP10.4.1, and 7.0-7.0 SP2.0.1). This vulnerability could expose user credentials on local workstations in environments where the Microsoft Edge web browser is used and user authentication is not configured with network accounts such as Active Directory or LDAP. This problem can expose user credentials to unauthorized third parties. If an unauthorized third party gains access to the workstation, patient data could be tampered with and system...

Classification

Class II

Category

medical device recall

Country

Japan

Agency

PMDA-DEVICE

Recall date

2026-02-27

Status

Ongoing

Official recall notice from PMDA-DEVICE

Recall details on Nibble Recalls: https://trynibble.app/recalls/c8032b75-3782-4166-8d3e-1b82bd6c7090