Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

IMRIS Operating Room table (ORT200 and ORT300). Intended for use Recalled by IMRIS Inc Due to One of the three pins that is used...

Date: October 1, 2014
Company: IMRIS Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact IMRIS Inc directly.

Affected Products

IMRIS Operating Room table (ORT200 and ORT300). Intended for use during diagnostic examinations or surgical procedures to support and position a patient.

Quantity: 14

Why Was This Recalled?

One of the three pins that is used to hold the ORT200 table alignment block in place on the floor of the MR Suite went missing during testing at a health care facility.

Where Was This Sold?

This product was distributed to 6 states: CA, FL, NH, NC, TN, UT

Affected (6 states)Not affected

About IMRIS Inc

IMRIS Inc has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report