Burnaby, Canada
A L I Technologies Ltd recalls
1 recall recorded since 2018, most recently on 2 December 2024. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 2 December 2024
- Reason
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-0958-2025, Z-0957-2025, Z-0959-2025
- Change Healthcare Cardiology Hemo software
- McKesson Cardiology Hemo software
- Change Healthcare Cardiology Hemodynamics software
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.