CHANGE HEALTHCARE CANADA COMPANY recalls Change Healthcare Cardiology Hemo Software

Due to complaints, software update may cause software to unexpectedly shutdown.

Change Healthcare Cardiology Hemo Software

On May 22, 2025, Change Healthcare issued a "Urgent Field Safety notice" to affected consignees via e-mail. On May June 11, 2025, Change Healthcare sent out an updated notification providing additional information. Change Healthcare asked consignees to take the following actions: 1. Change Healthcare has developed a software update that addresses this issue. Contact Change Healthcare support to schedule its deployment. 2. This notice must be distributed to all personnel within your organization who need to be aware of this notice. Customers should alert other affiliated parties that may be affected by this notice. 3. please maintain awareness of this Urgent Field Safety Notice until the issue has been fully resolved. 4. Please notify our Customer Support department that you have read and understood this field safety notice.

• FDA enforcement recordOfficial FDA database entry for Z-2071-2025
• FDA 510(k) clearance · K131497The device's official FDA premarket clearance record
• FDA device classification · MWIOfficial FDA classification for this device type
• CFR regulation · 21 CFR 870.2300The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find CHANGE HEALTHCARE CANADA COMPANYSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.