# FDA recall Z-0692-2018

> **Stryker Communications** · Class II · device recall initiated 2018-01-26.

## 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 (missing or incomplete) weld.

## Distribution

Distribution was made to medical facilities nationwide, including government and military distribution.  Foreign distribution was made to Canada, Belgium, China, United Kingdom, UAE, France, Germany, Spain, Japan, Ecuador, and Russia.

## Key facts

- **Recall number:** Z-0692-2018
- **Recalling firm:** Stryker Communications
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-26
- **Report date:** 2018-03-07
- **Termination date:** 2019-03-19

- **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-0692-2018

## Citation

> AI Analytics. FDA recall Z-0692-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0692-2018. Source: US FDA. Licensed CC0.

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