# FDA recall Z-2072-2025

> **CHANGE HEALTHCARE CANADA COMPANY** · Class II · device recall initiated 2025-05-22.

## Product

Change Healthcare Cardiology Hemodynamics Software

## Reason for recall

Due to complaints, software update may cause software to unexpectedly shutdown.

## Distribution

Worldwide - US Nationwide distribution in the states of AL, AR, CA, FL, KY MO, MS, NE, NH, NJ, PA, TN, TX, WA and the countries of Australia, Canada, Germany, Great Britain, Ireland, Israel, New Zealand.

## Key facts

- **Recall number:** Z-2072-2025
- **Recalling firm:** CHANGE HEALTHCARE CANADA COMPANY
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-22
- **Report date:** 2025-07-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Richmond, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2072-2025

## Citation

> AI Analytics. FDA recall Z-2072-2025. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-2072-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*