A L I Technologies Ltd: Device Recall
Recall #Z-0957-2025 · 12/02/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0957-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- A L I Technologies Ltd
- Status
- Ongoing
- Date Initiated
- 12/02/2024
- Location
- Burnaby, Canada
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 unit
Reason for Recall
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
Product Description
McKesson Cardiology Hemo software
Distribution Pattern
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.
Other Recalls by A L I Technologies Ltd
- Class II: Risk 12/02/2024
- Class II: Risk 12/02/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.