Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00) Recalled by Innovative Magnetic Resonance Imaging Systems Inc. Due to IMRIS Inc. initiated a recall of their OR...
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 Innovative Magnetic Resonance Imaging Systems Inc. directly.
Affected Products
IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and Neuro III-SV Magnetic Resonance Imaging Systems.
Quantity: 23
Why Was This Recalled?
IMRIS Inc. initiated a recall of their OR Tables ORT100 and ORT200. When proper procedure is not followed, the foot end of the IMRIS intra-operative OR table may be attracted to the MRI magnet as the magnet approaches the table. This poses a potential risk of injury to both the patient and operators standing near the table.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Innovative Magnetic Resonance Imaging Systems Inc.
Innovative Magnetic Resonance Imaging Systems Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report