# FDA recall Z-1602-2020

> **Stryker Communications** · Class II · device recall initiated 2019-10-11.

## Product

Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000

## Reason for recall

The firm has become aware that there is a likelihood that a missing snap ring or spanner nut may result in an insufficient mount force that causes the surgical light to fall. If the suspension of the surgical light falls, it may potentially cause serious injuries to Health Care Providers and/or patients.

## Distribution

US: Nationwide  OUS: Canada

## Key facts

- **Recall number:** Z-1602-2020
- **Recalling firm:** Stryker Communications
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-11
- **Report date:** 2020-04-08
- **Termination date:** 2022-10-18

- **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-1602-2020

## Citation

> AI Analytics. FDA recall Z-1602-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-1602-2020. Source: US FDA. Licensed CC0.

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