# FDA recall Z-1172-2021

> **Barco N.V.** · Class II · device recall initiated 2021-01-22.

## Product

Barco MDNC-3421 DISPLAY, DIAGNOSTIC RADIOLOGY

## Reason for recall

A number of MDNC-3421 displays were shipped while not being DICOM-compliant. These displays will not pass DICOM acceptance tests.

## Distribution

WI.

## Key facts

- **Recall number:** Z-1172-2021
- **Recalling firm:** Barco N.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-01-22
- **Report date:** 2021-03-10
- **Termination date:** 2022-11-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kortrijk, Belgium

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1172-2021

## Citation

> AI Analytics. FDA recall Z-1172-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1172-2021. Source: US FDA. Licensed CC0.

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