Change Healthcare Cardiology Hemodynamics software — Class II medical device recall Z-0959-2025
Ongoing recall by A L I Technologies Ltd, reported 2025-01-22, distributed nationwide. Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s
| Recall number | Z-0959-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | A L I Technologies Ltd, Burnaby, Canada |
| Recall initiated | 2024-12-02 |
| Classified | 2025-01-16 |
| Reported by FDA | 2025-01-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE, GB, IE, IL |
| Quantity | 2 units |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 17540262100129 |
Product
Change Healthcare Cardiology Hemodynamics software
Reason for recall
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0959-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.