# FDA recall Z-0762-2024

> **Getinge Usa Sales Inc** · Class II · device recall initiated 2023-11-08.

## Product

Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, OHDII FHD QL AIR03 E - ARD568803967, OHDII FHD QL AIR04 E/U - ARD568803968, OHDII FHD QL+ VP01 - ARD569204944, OHDII AIR03 QL FHD E - ARD568803951

## Reason for recall

A potential for a light system to fall in the operating room.

## Distribution

US Nationwide. Global Distribution.

## Key facts

- **Recall number:** Z-0762-2024
- **Recalling firm:** Getinge Usa Sales Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-08
- **Report date:** 2024-01-24

- **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-0762-2024

## Citation

> AI Analytics. FDA recall Z-0762-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0762-2024. Source: US FDA. Licensed CC0.

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