# FDA recall Z-2446-2019

> **Stryker Communications** · Class II · device recall initiated 2019-08-01.

## Product

Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light System.

## Reason for recall

The mounts on the monitor may have an insufficient weld.

## Distribution

Distribution was made to CA, CO, CT, FL, GA, IL, IN, MD, MI, MN, MO, NC, NH, NJ, NY, OH, PA, SC, TN, TX, and WI. There was foreign distribution to Canada and Germany.  There was no government/military distribution.

## Key facts

- **Recall number:** Z-2446-2019
- **Recalling firm:** Stryker Communications
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-01
- **Report date:** 2019-09-11
- **Termination date:** 2021-04-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Flower Mound, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2446-2019

## Citation

> AI Analytics. FDA recall Z-2446-2019. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2446-2019. Source: US FDA. Licensed CC0.

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