# FDA recall Z-2944-2020

> **Merge Healthcare, Inc.** · Class II · device recall initiated 2020-08-06.

## Product

Merge PACS

## Reason for recall

Measurements done on the Merge PACS generated MPR s may have incorrect measurements.

## Distribution

Domestic Distribution:  IL, MO, NY, ND, MI, TX, FL, OH, UT, NE, MS, MN, DE, AR, CA, WI, MD, NC, NH, GA, VA, SC, PE, CT, NM, IN.    International Distribution: CA, BE, UK.

## Key facts

- **Recall number:** Z-2944-2020
- **Recalling firm:** Merge Healthcare, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-06
- **Report date:** 2020-09-16
- **Termination date:** 2022-11-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hartland, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2944-2020

## Citation

> AI Analytics. FDA recall Z-2944-2020. Retrieved 2026-06-15 from https://api.ai-analytics.org/recall/Z-2944-2020. Source: US FDA. Licensed CC0.

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