FDA Device recall Z-1466-2022
Centricity PACS Software Version 7.0 SP0.0.4.7
- FDA Device
- Class II
- terminated
- Published 2022-08-03
On 2022-08-03 the FDA classified a Class II recall of Centricity PACS Software Version 7.0 SP0.0.4.7 by Ge Healthcare, citing the Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1466-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-06-14 |
| Published | 2022-08-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Centricity PACS Software Version 7.0 SP0.0.4.7
Reason
The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.
Identifiers
| code_info | Model: 5831882-012, Software Version 7.0 SP0.0.4.7 GTIN: 00840682145572 |
|---|
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-1466-2022%22
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