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A L I Technologies Ltd recalls Change Healthcare Cardiology Hemo software
Recalled January 22, 2025 · FDA recall Z-0958-2025 · A L I Technologies
Hazard
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s). · FDA Class II
Units
204 units
Sold at
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.
Description
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
Product
Change Healthcare Cardiology Hemo software
Manufacturer(s)
A L I Technologies Ltd
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →