# FDA recall Z-3034-2026

> **IMRIS Imaging Inc** · Class II · device recall initiated 2026-08-06.

## Product

ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600

## Reason for recall

The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement occurs during a procedure.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden.

## Key facts

- **Recall number:** Z-3034-2026
- **Recalling firm:** IMRIS Imaging Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-08-06
- **Report date:** 2026-09-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chaska, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3034-2026

## Citation

> MORVS. FDA recall Z-3034-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-3034-2026. Source: US FDA. Licensed CC0.

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