Use caution Medical device recall · FDA · Published February 20, 2018

Deerfield Imaging IMRIS T2X Table Recall: Risk of Unintended Movement

Deerfield Imaging recalls IMRIS T2X surgical tables with serial numbers listed. The rotational locking may disengage during use, causing unintended table movement. Affected users should contact for remedy.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0976-2018Medical device Deerfield Imaging ›

Use caution until it’s fixed

The rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked while in use which could potentially result in unintended movement of the table.

Take action

Contact the company

Recalling firmDeerfield Imaging, Inc.5101 Shady Oak Rd S · Minnetonka, MN 55343-4100

✎ GovInfoNow plain-language explainer

Deerfield Imaging is recalling specific IMRIS T2X surgical tables due to a risk that the rotational locking mechanism could become unlocked while in use, potentially causing unintended table movement. This could lead to patient safety issues during medical procedures. Read more at govinfonow.com/recall/71933-deerfield-imaging-imris-t2x-table-recall-risk-of-unintended-movement.

Source Summary by GovInfoNow · govinfonow.com/recall/71933-deerfield-imaging-imris-t2x-table-recall-risk-of-unintended-movement · Updated August 28, 2026 · FDA enforcement record: FDA #Z-0976-2018

Cite this page

“Deerfield Imaging IMRIS T2X Table Recall: Risk of Unintended Movement.” GovInfoNow, updated August 28, 2026. https://govinfonow.com/recall/71933-deerfield-imaging-imris-t2x-table-recall-risk-of-unintended-movement. Based on FDA recall #Z-0976-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0976-2018%22&limit=1).

The FDA announced on Feb. 20, 2018, that Deerfield Imaging, Inc. is recalling IMRIS T2X Tables due to a hazard of unintended movement. The agency stated the rotational locking mechanisms can become disengaged while in use.

How to tell if you have it

Brand: Deerfield Imaging
Product: IMRIS T2X Table
Part Number: 109682-600
Serial Numbers: 10000239, 10001306, 10000983, 10000982, 10000233, 10001119, 10001192, 10002375, 10003623, 10003623, 05 002, 10003634, 10001118, 10001188, 10001340, 10003638
Quantity: 16 tables

The hazard

According to the FDA, the rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked while in use. This defect could potentially result in unintended movement of the table.

Context

GovInfoNow's records show Deerfield Imaging, Inc. has had 8 other recalls since Feb. 23, 2018. Other recent recalls include a Feb. 17, 2022 recall for HFD100 Head Fixation Components and an Aug. 25, 2021 recall for ORT200/300 Operating Room Tables. Similar recent recalls of operating room tables include the IMRIS ORT300 (Aug. 6, 2026) and IMRIS ORT200 (Aug. 6, 2026).

How to tell if you have this one

Check the serial number on the table's label. The recalled models have specific serial numbers listed in the recall notice, including 10000239, 10001306, and others.

Brand
Deerfield Imaging
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Terminated
Distribution
US, Canada, Australia, China, Qatar

Recall number	Product, codes & lots	Quantity
Z-0975-2018	IMRIS ORT100 Table, Part Number 110470-000; Serial Numbers: 10002341, 10003629, 10003801, 10002654, 10002795, 10002796, 10002847, 10003830, 10003243, 10002848, 10003241, 10005651, 10007348, 10007424, 10006886	15 tables
Z-0976-2018	IMRIS T2X Table, Part Number 109682-600; Serial Numbers: 10000239, 10001306, 10000983, 10000982, 10000233, 10001119, 10001192, 10002375, 10003623, 10003623, 05 002, 10003634, 10001118, 10001188, 10001340, 10003638	16 tables

Based on the official FDA remedy

What to do — step by step

Check Serial Number
Look for the serial number on the table's label to confirm if it is in the list of recalled numbers.

How this recall unfolded

Recall timeline

FDA terminated this recall 18 months after the firm started it.

Feb 20, 2018Firm started the recall
Mar 13, 2018FDA classified it Class II
Mar 21, 2018Published in FDA’s Enforcement Report
Aug 27, 2019FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/71933-deerfield-imaging-imris-t2x-table-recall-risk-of-unintended-movement">Deerfield Imaging IMRIS T2X Table Recall: Risk of Unintended Movement (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0976-2018 (February 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0976-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 28, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.