# FDA recall Z-2620-2017

> **Merge Healthcare, Inc.** · Class II · device recall initiated 2017-05-24.

## Product

Merge OrthoPACS software.

## Reason for recall

A migrated study that has annotations will display the annotations, but when a prior study is loaded that should have annotations, the second study will not display annotations.

## Distribution

Distribution was made nationwide to medical facilities.  There was no foreign/government/military distribution.

## Key facts

- **Recall number:** Z-2620-2017
- **Recalling firm:** Merge Healthcare, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-24
- **Report date:** 2017-06-28
- **Termination date:** 2019-06-28

- **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-2620-2017

## Citation

> AI Analytics. FDA recall Z-2620-2017. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-2620-2017. Source: US FDA. Licensed CC0.

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