Medical Device Recall: Change Healthcare Cardiology Hemodynamics software
A L I Technologies Ltd · December 2, 2024
Reason for Recall
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
Distribution
US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, PA, SC, SD, TN, TX, WA, WI and the countries of Australia, Israel, Canada, Germany, Ireland, United Kingdom.
States Affected
NATIONWIDE
Quantity Affected
2 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0959-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.