Recall Z-0128-2025

Change Healthcare Canada Company · initiated August 21, 2024

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

McKesson Cardiology Hemo. Versions 13.0, 13.1.1, 13.1.2, 13.2, 13.2.1, 14.0.

Codes / lots: UDI Numbers: (01)80010939050010(10)130201, (01)80010939050027(10)140000. Versions Versions 13.0, 13.1.1, 13.1.2, 13.2, 13.2.1, 14.0.

Reason for recall

A potential issue has been identified in Change Healthcare Cardiology Hemo where incorrect data entry can lead to inaccurate hemodynamic calculations, potentially resulting in misdiagnosis and inappropriate treatment. This issue occurs when the unit of measurement (UOM) for hemoglobin is configured in a way that differs from the users understanding.

FDA-determined cause: Use error

Action taken

Change Healthcare notified consignees on about 08/21/2024 via emailed letter. Consignees were instructed to pay careful attention to the hemoglobin unit of measurement displayed on the top of the "results" screen of the Hemo application, communicate the issue to all relevant team members to ensure vigilance in data entry, ensure that the hemoglobin values are entered in the correct unit of measurement (mmol/l or g/dl) as configured in the Management Console and displayed at the top of the results screen, contact Change Healthcare support to schedule the deployment of the software update that addresses this issue. Additionally, consignees were requested to complete and return the response form. With regard to potentially affected data, Change Healthcare recommended consignees verify f the UOM setting for hemoglobin is configured to what users would expect, if the UOM settings are different than expected, contact Change Healthcare support for assistance with identifying when the UOM setting was changed, and which procedures were affected, and examine affected procedures and implement necessary corrective actions to rectify the data and address patient care concerns.

Details

Recall number
Z-0128-2025
Initiated
August 21, 2024
Posted by FDA
October 17, 2024
Product code
DQK – Computer, Diagnostic, Programmable
Quantity
35 systems
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Canada, Germany, Ireland, Israel, United Kingdom.
Recalling firm
Change Healthcare Canada Company, Richmond

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0126-2025 Class IIChange Healthcare Cardiology Hemo. Versions 14.2, 14.1.1, 14.2, 14.3, 14.3.2, 14.3…A potential issue has been identified in Change Healthcare Cardiology Hemo where incorrect data entry can… 08/21/2024Open, Classified
Z-0127-2025 Class IIHorizon Cardiology Hemo. Version 12.2.A potential issue has been identified in Change Healthcare Cardiology Hemo where incorrect data entry can… 08/21/2024Open, Classified