# FDA recall Z-2585-2021

> **Deerfield Imaging, Inc.** · Class II · device recall initiated 2021-08-25.

## Product

Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.

## Reason for recall

ORT200/300 rotational lock may fail to function such that it cannot change states between locked and unlocked, due to a mechanical hardware issue.

## Distribution

Worldwide distribution - US Nationwide distribution  FL, NH, TX, OH, CA, OR, UT, TN, NC and the countries of Canada, Australia, Sweden, Japan.

## Key facts

- **Recall number:** Z-2585-2021
- **Recalling firm:** Deerfield Imaging, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-08-25
- **Report date:** 2021-10-06
- **Termination date:** 2024-04-30

- **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-2585-2021

## Citation

> AI Analytics. FDA recall Z-2585-2021. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-2585-2021. Source: US FDA. Licensed CC0.

---

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