Data Foundry

Medical device recalls 2022

Centricity PACS Software Version 7 — Class II medical device recall Z-1466-2022

Terminated recall by GE Healthcare, LLC, reported 2022-08-03, distributed nationwide. The Event Notification Manager (ENM) functionality for certain products does not process notifications for stu

Recall numberZ-1466-2022
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmGE Healthcare, LLC, Waukesha, WI, United States
Recall initiated2022-06-14
Classified2022-07-25
Reported by FDA2022-08-03
Terminated2024-01-16
DistributedNationwide (US)
Countries outside the USBR, CA, CH, CN, DE, ES, FR, GB, IL, IT, JP, OM
Quantity47 installations
UPC / GTIN / UDI-DI00840682145572
Model numbers5831882-012

Product

Centricity PACS Software Version 7.0 SP0.0.4.7

Reason for recall

The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1466-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.