Use caution Medical device recall · FDA · Published August 25, 2021

Deerfield Imaging ORT200/300 Operating Room Table Recall: Rotational Lock May Fail

Deerfield Imaging recalls ORT200/300 operating room tables with a rotational lock that may fail to lock or unlock properly, posing a risk of patient injury during procedures.

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

🇺🇸 FDA recall #Z-2585-2021Medical device Deerfield Imaging ›

Use caution until it’s fixed

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

Take action

Contact the company

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

✎ GovInfoNow plain-language explainer

Deerfield Imaging recalls certain operating room tables (ORT200/300 models) because their rotational lock might not function correctly, potentially causing the table to become stuck in a position during medical procedures. This could lead to patient injury if the table cannot be adjusted safely. Read more at govinfonow.com/recall/61895-deerfield-imaging-ort200-300-operating-room-table-recall-rotational-lock.

Source Summary by GovInfoNow · govinfonow.com/recall/61895-deerfield-imaging-ort200-300-operating-room-table-recall-rotational-lock · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2585-2021

Cite this page

“Deerfield Imaging ORT200/300 Operating Room Table Recall: Rotational Lock May Fail.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61895-deerfield-imaging-ort200-300-operating-room-table-recall-rotational-lock. Based on FDA recall #Z-2585-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2585-2021%22&limit=1).

Deerfield Imaging, Inc. recalled its Operating room table due to a mechanical hardware issue that may prevent the rotational lock from functioning, according to the FDA on 2021-08-25.

How to tell if you have it

Brand: Deerfield Imaging
Model Number: 114093-000
Serial Numbers: 10005695, 10002998, 10005456, 10007377, 10002997, 10006737, 10004372, 10002841, 10005613, and 10002255

The hazard

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

Context

GovInfoNow's records show Deerfield Imaging, Inc. has 8 other recalls on record since 2018-02-20. Other recent recalls of similar products include IMRIS ORT300 Operating Room Table Recall (2026-08-06), IMRIS ORT200 Operating Room Table Recall (2026-08-06) and Philips Azurion 3 M15 System Recall (2026-01-26).

How to tell if you have this one

Check for the model number 114093-000 and serial numbers listed in the recall (e.g., 10005695, 10002998). These tables were sold with specific serial numbers between 2019 and 2020.

Brand
Deerfield Imaging
Category
Medical device

FDA recall event · 3 products

All 3 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
Worldwide distribution - US Nationwide distribution FL, NH, TX, OH, CA, OR, UT, TN, NC and the countries of Canada, Australia, Sweden, Japan.

Recall number	Product, codes & lots	Quantity
Z-2584-2021	Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.; UDI: 00857534006738 and 00857534006349 Model Number: 113821-000 (Serial Number: 10002220); Model Number: 113821-600 (Serial Numbers: 10002692, 10006152, 10006991, 10004513, 10006997, and 10003754); Model Number: 114148-000 (Serial Numbers: 10004463, 10006891, 10005189, 10005190, 10004327, and 10004997)	13 units
Z-2585-2021	Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.; UDI: 00857534006356 Model Number: 114093-000; Serial Numbers: 10005695, 10002998, 10005456, 10007377, 10002997, 10006737, 10004372, 10002841, 10005613, and 10002255.	10 units
Z-2586-2021	Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.; UDI: 00857534006462; Model Number: 114093-600; Serial Number: 10007411, 10002996, 10004515.	3 units

Based on the official FDA remedy

What to do — step by step

Check Table Status
Verify if the rotational lock functions correctly by attempting to lock and unlock it manually.
Contact Manufacturer
Reach out to Deerfield Imaging for guidance on whether the table needs repair or replacement.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 9 states.

FDA distribution: “Worldwide distribution - US Nationwide distribution FL, NH, TX, OH, CA, OR, UT, TN, NC and the countries of Canada, Australia, Sweden, Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: California, Florida, New Hampshire, North Carolina, Ohio, Oregon, Tennessee, Texas, Utah.

Recall timeline

FDA terminated this recall 2.7 years after the firm started it.

Aug 25, 2021Firm started the recall
Sep 28, 2021FDA classified it Class II
Oct 6, 2021Published in FDA’s Enforcement Report
Apr 30, 2024FDA terminated the recall

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

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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/61895-deerfield-imaging-ort200-300-operating-room-table-recall-rotational-lock">Deerfield Imaging ORT200/300 Operating Room Table Recall: Rotational Lock May Fail (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-2585-2021 (August 25, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2585-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.