# FDA recall Z-0160-2024

> **Omega Medical Imaging, Inc.** · Class II · device recall initiated 2023-09-08.

## Product

Omega Medical Imaging Elevating Monitor Suspension Systems, Part Number 1000-0085

## Reason for recall

An actuator separated from the pivot mechanism on a lower monitor boom system column. The lower boom became detached at the point shown and was restrained by the installed safety cable.

## Distribution

Alabama, California, Illinois, Indiana, Kentucky, Louisiana, Missouri, Montana, North Carolina, Ohio, Oklahoma

## Key facts

- **Recall number:** Z-0160-2024
- **Recalling firm:** Omega Medical Imaging, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-08
- **Report date:** 2023-11-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sanford, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0160-2024

## Citation

> AI Analytics. FDA recall Z-0160-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0160-2024. Source: US FDA. Licensed CC0.

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