FDA Device recall Z-1229-2022
Centricity Universal Viewer Zero Footprint Client
- FDA Device
- Class II
- ongoing
- Published 2022-06-15
On 2022-06-15 the FDA classified a Class II recall of Centricity Universal Viewer Zero Footprint Client by Ge Healthcare, citing potential for Distance and Area measurements to display inaccurate measurement values when performed on magnified images, and specific to ZFP, Distance and Area measurements can d….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1229-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-04-28 |
| Published | 2022-06-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Centricity Universal Viewer Zero Footprint Client
Reason
Potential for Distance and Area measurements to display inaccurate measurement values when performed on magnified images, and specific to ZFP, Distance and Area measurements can display inaccurate measurement values when performed on lossy images that are scaled down from their original resolution.
Identifiers
| code_info | Software Version 6.0 SP11 through 6.0 SP11.4; GTIN/DI: 00840682102988; Codes: 2089507-1XX |
|---|
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-1229-2022%22
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