Z-1333-2022 Class II Ongoing
FDA device recall Z-1333-2022 was initiated by GE Healthcare, LLC on Jun 8, 2022 and is designated Class II. Reason for recall: Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP) The recall status is ongoing. Affected quantity: 1,934 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 13, 2022
- Initiation Date
- Jun 8, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,934 units
Product Description
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 for Recall
Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)
Distribution Pattern
Worldwide distribution.
Code Information
UDI 00840682102988, Versions 6.0 SP6 through SP11.4
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1333-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026