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

Recall Z-1402-2025 — Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.1, 12.1.1, 12.2, 12.3, 12.3.1, 12.3.2, 12.3.3, 12.4, 12.4.1, 12.4.2; Merge Cardio is a software medical device that is an integrated multi-modality image cardiovascular information management system.

U.S. FDA — Device Enforcement · United States · 2025-02-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1402-2025
Date of alert
2025-02-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Merge Healthcare, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00842000101123
Reported risk: When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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