# FDA recall Z-0989-2019

> **GETINGE US SALES LLC** · Class II · device recall initiated 2019-01-08.

## Product

Maquet XS Flat Screen Monitor Holder, PWD70+DF HD R XS32 K3 SPE, Configuration Part Number ARD268400150A    Product Usage:  This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.

## Reason for recall

The affected flat screen monitor holders might not be compliant with grounding requirements. As a consequence, there is a risk of mild to severe/fatal electric shock under certain conditions while using the flat screen monitor holder with voltage of 100-220V.

## Distribution

The products were distributed to the following US states:  AZ and TX.

## Key facts

- **Recall number:** Z-0989-2019
- **Recalling firm:** GETINGE US SALES LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-08
- **Report date:** 2019-03-13
- **Termination date:** 2020-06-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wayne, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0989-2019

## Citation

> AI Analytics. FDA recall Z-0989-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0989-2019. Source: US FDA. Licensed CC0.

---

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