# FDA recall Z-1508-2021

> **CHANGE HEALTHCARE CANADA COMPANY** · Class II · device recall initiated 2021-03-17.

## Product

Change Healthcare Enterprise Viewer

## Reason for recall

Change Healthcare has identified an intermittent software defect which may result in an anchor study failing to display.

## Distribution

Domestic Distribution only. IN, KY, CA, NY, WA, IL, IA, FL, TX, WA, MI, HI, AK, WI, WY, NE, AZ, OH, PA

## Key facts

- **Recall number:** Z-1508-2021
- **Recalling firm:** CHANGE HEALTHCARE CANADA COMPANY
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-03-17
- **Report date:** 2021-05-05

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1508-2021

## Citation

> AI Analytics. FDA recall Z-1508-2021. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1508-2021. Source: US FDA. Licensed CC0.

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