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

Recall Z-1508-2021 — Change Healthcare Enterprise Viewer

U.S. FDA — Device Enforcement · Canada · 2021-03-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1508-2021
Date of alert
2021-03-17
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
CHANGE HEALTHCARE CANADA COMPANY
Product category
device
Product type
Devices
Reported risk: Change Healthcare has identified an intermittent software defect which may result in an anchor study failing to display.
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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