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

Recall Z-0289-2021 — Merge LIS

U.S. FDA — Device Enforcement · United States · 2017-01-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0289-2021
Date of alert
2017-01-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Merge Healthcare, Inc.
Product category
device
Product type
Devices
Reported risk: A defect in the software resulted in medications that are not associated with the patient (i.e., medications that the patient is not currently taking) appearing on their report.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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