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.
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FDA Device · Class II · 2026-09-23 · Ge Healthcare - Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Adminis…
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise im…
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions
FDA Device · Class II · 2026-09-23 · Ge Healthcare - Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions
FDA Device · Class II · 2026-09-23 · Ge Healthcare
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1466-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.