Recall Z-2072-2025— CHANGE HEALTHCARE CANADA COMPANY

Class II · Ongoing

Class II FDA medical device recall by CHANGE HEALTHCARE CANADA COMPANY, initiated 2025-05-22. It names one FDA 510(k) clearance: K230881. Product: Change Healthcare Cardiology Hemodynamics Software. Reason: Due to complaints, software update may cause software to unexpectedly shutdown..

Recalling firm
CHANGE HEALTHCARE CANADA COMPANY
Classification
Class II
Status
Ongoing
Initiated
2025-05-22
Firm location
Richmond, Canada

510(k) clearances named in this recall

1 on FDA's record

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Change Healthcare Cardiology Hemodynamics Software

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.