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MEDICAL DEVICE RECALLMODERATE

Centricity Universal Viewer Software

GE recalls Centricity Universal Viewer software over credential exposure risk.

What to do

Contact GE Medical Systems for software update instructions to remediate the vulnerability.

Recalled
Listed
Updated
Recall No.
Z-1571-2026
Agency
FDA
Firm
GE Medical Systems, LLC
Recall ID
98428
Status
ONGOING

Why it was recalled

GE Medical Systems is recalling Centricity Universal Viewer Software versions 5.0 SP6 through UV 5.0 SP7.1 due to a cybersecurity vulnerability that may expose user login credentials on the local client workstation, potentially allowing unauthorized individuals to impact system availability or manipulate data.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

Centricity Universal Viewer Software Versions

ProductRecall #UDI-DI
5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2089629-003, 2066908-136, 2066908-150Z-1571-202600558643, 00558700, 00558694, 00558103, 00558677, 00558340, 00558682, 01431499, 02176369, 01454622, 00158976, 00044549, 00071707, 25540620, 00001393, 00260808, 00157857, 01282268, 01820534, 01820555
7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 5826659-029, 5826659-032, 5826659-033, 5826659-028, 5826659-034, 5826659-030, 5826659-019, 5826659-022, 5826659-026, 5826659-023, 5826659-031, 5826659-025, 5826659-002, 5826659-021, 5826659-037, 5826659-014, 5826659-016, 5826659-013Z-1569-202600840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794, 00840682145794
6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 2100491-006, 2088026-723, 2088026-308, 2104867-044, 2100491-012, 2088026-962, 2088026-969, 2102676-001, 2088026-936, 2088026-960, K1220JWED, 2088026-806, 2088026-506, 2088026-026, 2088026-970, 2088026-943, 2088026-990, 2088Z-1570-202600840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800, 00840682103800
6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 2100491-006, 2088026-723, 2088026-308, 2104867-044, 2100491-012, 2088026-962, 2088026-969, 2102676-001, 2088026-936, 2088026-960, K1220JWED, 2088026-806, 2088026-506, 2088026-026, 2088026-970, 2088026-943, 2088026-990, 2088026-940, 2088026-959, 2088026-967, 2088026-989, 2104867-045, 2088026-993, 2088026-306, 2102675-010, 2088026-948, 2088026-957, 2088026-973, 2088026-946, 2088026-715, 2088026-906––

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-07-28 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification