Home / Recalls / Medical Devices
GE Healthcare recalls Centricity Universal Viewer, Centricity Universal Viewer 6.0, Model/Catalog Numbers: a) 2088026-003, b) 2088026-026,
Recalled May 10, 2023 · FDA recall Z-1501-2023 · GE Healthcare
Hazard
GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information. · FDA Class II
Units
329 units
Sold at
Worldwide Distribution
Description
GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information.
Product
Centricity Universal Viewer, Centricity Universal Viewer 6.0, Model/Catalog Numbers: a) 2088026-003, b) 2088026-026, c) 2088026-032, d) 2088026-043, e) 2088026-044, f) 2088026-115, g) 2088026-132, h) 2088026-306, i) 2088026-308, j) 2088026-406, k) 2088026-506, l) 2088026-613, m) 2088026-713, n) 2088026-714, o) 2088026-723, p) 2099714-001, q) 2100169-001, r) 2100491-006, s) 2102675-010, t) 2102676-001, u) 2104867-044, v) 2104867-045; Radiological Image Processing System
Manufacturer(s)
GE Healthcare
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →