---
title: "Change Healthcare Cardiology Hemodynamics software — FDA record Z-0959-2025 | Is It on Recall"
description: "Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s)."
url: https://isitonrecall.com/recall/fda-device-z-0959-2025-change-healthcare-cardiology-hemodynamics-software/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Change Healthcare Cardiology Hemodynamics software — FDA record Z-0959-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 2, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Change Healthcare Cardiology Hemodynamics software
- **Reason**: Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
- **Classification**: Class II
- **Recalling firm**: A L I Technologies Ltd
- **Quantity**: 2 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0959-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0959-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Software version 15.01/UDI:(01)17540262100129 |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jan 22, 2025
- **Recall initiation date**: Dec 2, 2024
- **Center classification date**: Jan 16, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0959-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [A L I Technologies Ltd records](https://isitonrecall.com/brand/a-l-i-technologies-ltd/)