Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0722-2023 — Centricity Universal Viewer 6.0. Used to display medical images (Including mammograms) and data from various imaging sources.

U.S. FDA — Device Enforcement · United States · 2022-10-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0722-2023
Date of alert
2022-10-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Medical Systems, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
14194768
Reported risk: There is the potential that after installation of the IAS tool, some studies can remain hidden without user notification. Access to those hidden studies requires GE Healthcare assistance, which can result in a delay in reading the study.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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