VERICIS, Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.0.1, 12.0.2; The VERICIS is an integrated cardiovascular information system classified as a picture archiving and communications system.
FDA Recall Z-1401-2025 · Posted 2025-03-20
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Recalling FirmMerge Healthcare, Inc.
Recall StatusOpen, Classified
Product CodeLLZ
Date Initiated2025-02-19
Product Quantity37
Reason for Recall
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.
Firm Action
Merge Healthcare issued an Urgent Field Safety Notice to it's consignees on 02/19/2025 via email. The notice explained the issue, risk to patients, provided a workaround to immediately address the issue, and recommended clinicians check measurements in the final report to ensure that they accurately reflect the patient's condition pending software update.
Required Actions:
Merge Healthcare Support will contact all customers to:
i) Confirm that you have read and understood this Urgent Field Safety Notice.
ii) Schedule an update to implement the configuration change on your system.
For more information, please contact Merge Healthcare Support at 1-877-741-5369 (available 24 hours a day, 7 days a week) or visit our website: https://www.merative.com/support/merge.
Please forward this notice to any individuals within your organization that may need to be aware of this notification. Customers should alert any other affiliated parties that may be affected by this Urgent Field Safety Notice.
The firm identified a missing software version (11.0.2) and issued the corrected notice on 03/03/2025.
Root Cause
Software design
Distribution Pattern
US
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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