FDA Device recall Z-0329-2022
GE Centricity Universal Viewer Zero Footprint Client
- FDA Device
- Class II
- terminated
- Published 2021-12-08
On 2021-12-08 the FDA classified a Class II recall of GE Centricity Universal Viewer Zero Footprint Client by Ge Healthcare, citing there is a potential to display incomplete patient imaging study.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0329-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-10-15 |
| Published | 2021-12-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
GE Centricity Universal Viewer Zero Footprint Client
Reason
There is a potential to display incomplete patient imaging study.
Identifiers
| code_info | Versions 6.0 SP9, SP9.0.1, SP9.0.1.1, SP9.0.1.2, SP9.0.1.3, SP9.0.1.4, SP9.0.1.5, SP10, SP10.1, SP10.2, SP10.2.1, SP10.…Versions 6.0 SP9, SP9.0.1, SP9.0.1.1, SP9.0.1.2, SP9.0.1.3, SP9.0.1.4, SP9.0.1.5, SP10, SP10.1, SP10.2, SP10.2.1, SP10.2.1.1, SP10.2.2, SP10.2.2.1 configured with a Centricity PACS back end. GTIN 00840682102988; UDI 00840682102988. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0329-2022%22
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