Recall archive / FDA device enforcement
Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions — FDA record Z-3169-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jul 31, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions
- Reason
- Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.
- Classification
- Class II
- Recalling firm
- GE Healthcare
- Quantity
- 116 systems
- Agency-reported status
- Ongoing
- Source record identifier
- Z-3169-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: 00195278882585; System IDs: 847NWCPVSW 847NWCPVSW2 NORTHWEST25206018 207795PVSWC3 207795PVSWC1 207795PVSWC2 604520GEPACS 613548IMSA 613548IMSB 613548TESTIMS 613548GEPACS EG1055PC01 B4191728 C4191734 D4191718 E4191720 tobecreated HHEI02CS01 UC1989CS01 CPACS Testsystem Not Available HCIT5592143PACS JL1758 JD1266 JL1760 JAS004 JL1762 JAS042 JL1757 JL1761 JL1759 KW1018PP01 ALRAZIIMS LB1279PC02 BMALTA25 PIV-PIMS1 SA2591PP01 SA2039PP01 SA2315PP12 KAMCJIMS2 SA1208PP01 SA2000PP01 SA1006PP07 KFHIMS2 KAHIMS2 MKNSHIMS2 ZA2895PACS02 FEG85600 FEG85608 FEG34405 FEG34406 FEB92518 FEB92519 FEE07A22 FEE07A23 FEG85700 FEG85704 FE410911 FE410912 IMSTEST TBC DE619840 DE619846 DEM88511 DEM88512 DEM87116 DEM87121 DEI12311 DEI12312 DEP00203 20034126 NE465120 NE670325 NE673137 NE300609 NE219643 FE816139 FE816140 FE8161102 DPP03300 DPP03301 DPP03302 DPP03303 DPP03305 FEG51800 FEF70522 FEF70523 MEX61704 MEX67314 GPX24300 NPV73804 25277590 NE203141 NE740521 NE216225 NE487826 MEX67605 NE723605 NEV07027 NE748614 NEV13618 NEV06838 NE304907 NE223245 NE419140 NEV44001 NPV84521 NEV44017 NEV44018 NEV44034 NE741437 NEV35826 NE688826 GEE34022 06002PAC37 06051PAC01 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide - US Nationwide distribution.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Sep 23, 2026
- Recall initiation date
- Jul 31, 2026
- Center classification date
- Sep 15, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.