Recall archive / FDA device enforcement
GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data wit... — FDA record Z-1333-2022
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 Jun 8, 2022. 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
- GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data within a computer network or on a workstation.
- Reason
- Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)
- Classification
- Class II
- Recalling firm
- GE Healthcare, LLC
- Quantity
- 1,934 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1333-2022
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 00840682102988, Versions 6.0 SP6 through SP11.4 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide distribution.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Jul 13, 2022
- Recall initiation date
- Jun 8, 2022
- Center classification date
- Jul 5, 2022
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.