Class II — A L I Technologies Ltd
| Recalling firm | K&R Technologies dba Microbiology International |
|---|---|
| Registered facility | K&R TECHNOLOGIES DBA MICROBIOLOGY INTERNATIONAL (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s). |
| Product | McKesson Cardiology Hemo software |
| Quantity | 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. |
| Initiated | 2024-12-02 |
| Classified | 2025-01-16 |
| Recall number | Z-0957-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — A L I Technologies Ltd (Z-0957-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96025/
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