# FDA recall Z-2601-2017

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

## Product

Merge OrthoPACS software.  The firm name on the label is Merge Healthcare, Hartland, WI.

## Reason for recall

Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate via telmed protocol to the destination server and may fail to import on the destination server.

## Distribution

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

## Key facts

- **Recall number:** Z-2601-2017
- **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:** 2019-10-15

- **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-2601-2017

## Citation

> AI Analytics. FDA recall Z-2601-2017. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2601-2017. Source: US FDA. Licensed CC0.

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