# FDA recall Z-1218-2018

> **Deerfield Imaging, Inc.** · Class II · device recall initiated 2018-02-23.

## Product

IMRIS ORT300 Removable Operating Room Table, 50-60 Hz Version is intended for use during diagnostic examinations or surgical procedures to support and position a patient.

## Reason for recall

The rotational locking mechanisms on the ORT 200/300 tables fail to operate such that it cannot change states between locked and unlocked.

## Distribution

US, Canada, China, Sweden, Germany, Japan, Qatar, France, Audtralia

## Key facts

- **Recall number:** Z-1218-2018
- **Recalling firm:** Deerfield Imaging, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-02-23
- **Report date:** 2018-04-04
- **Termination date:** 2019-08-27

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1218-2018

## Citation

> AI Analytics. FDA recall Z-1218-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1218-2018. Source: US FDA. Licensed CC0.

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