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

Recall Z-1773-2021 — Change Healthcare Enterprise Viewer - Product Usage: intended to be used with off-the-shelf hardware for the 2D and 3D display of DICOM and non-DICOM medical images, reports, and multimedia content.

U.S. FDA — Device Enforcement · Canada · 2021-04-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1773-2021
Date of alert
2021-04-19
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
CHANGE HEALTHCARE CANADA COMPANY
Product category
device
Product type
Devices
Reported risk: A software defect was identified where the Image Styles defined by presentation states from CHRS are not displayed in CHEV.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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