PlainRecalls
FDA Devices Moderate Class II Ongoing

McKesson Cardiology Hemo software

Reported: January 22, 2025 Initiated: December 2, 2024 #Z-0957-2025

Product Description

McKesson Cardiology Hemo software

Reason for Recall

Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).

Details

Recalling Firm
A L I Technologies Ltd
Units Affected
1 unit
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.
Location
Burnaby

Frequently Asked Questions

What product was recalled?
McKesson Cardiology Hemo software. Recalled by A L I Technologies Ltd. Units affected: 1 unit.
Why was this product recalled?
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
Which agency issued this recall?
This recall was issued by the FDA Devices on January 22, 2025. Severity: Moderate. Recall number: Z-0957-2025.