FDA Device recall Z-1333-2022
GE Centricity Universal Viewer Zero Footprint
- FDA Device
- Class II
- ongoing
- Published 2022-07-13
On 2022-07-13 the FDA classified a Class II recall of GE Centricity Universal Viewer Zero Footprint by Ge Healthcare, citing potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1333-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-06-08 |
| Published | 2022-07-13 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ge Healthcare |
| Distribution | n/a |
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)
Identifiers
| code_info | UDI 00840682102988, Versions 6.0 SP6 through SP11.4 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1333-2022%22
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