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.
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