Skip to content
Get alerts
GovInfoNow
Use caution Medical device recall · FDA · Published February 23, 2018

Deerfield Imaging IMRIS ORT300 Operating Room Table Recall: Drifting Table Hazard

Deerfield Imaging recalls IMRIS ORT300 operating room tables with specific part numbers and serials due to potential unintended movement during use. Affected users should contact the manufacturer for details.

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

🇺🇸 FDA recall #Z-1266-2018Medical deviceDeerfield Imaging ›
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 IMRIS ORT300 operating room tables that may drift while in use, which could cause unintended movement. This hazard poses a risk to surgical procedures and patient safety. Read more at govinfonow.com/recall/71875-deerfield-imaging-imris-ort300-operating-room-table-recall-drifting-table.

Source Summary by GovInfoNow · govinfonow.com/recall/71875-deerfield-imaging-imris-ort300-operating-room-table-recall-drifting-table · Updated August 27, 2026 · FDA enforcement record: FDA #Z-1266-2018

Cite this page

“Deerfield Imaging IMRIS ORT300 Operating Room Table Recall: Drifting Table Hazard.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/71875-deerfield-imaging-imris-ort300-operating-room-table-recall-drifting-table. Based on FDA recall #Z-1266-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1266-2018%22&limit=1).

Deerfield Imaging, Inc. recalled IMRIS ORT300 removable operating room tables with specific part and serial numbers due to a potential drift hazard, according to the Food and Drug Administration on Feb. 23, 2018.

How to tell if you have it

  • Brand: Deerfield Imaging
  • Product: IMRIS ORT300 Removable Operating Room Table
  • Part Numbers: 114093-000, 114093-600
  • Serial Numbers (Part 114093-000): 10005695, 10002998, 10005456, 10007377, 10002997, 10005612, 10004372, 10002841, 10002255, 10005613
  • Serial Numbers (Part 114093-600): 10007411, 10002996, 10004515

The hazard

The operating room table may drift while in use, which could potentially result in unintended movement of the table.

Context

GovInfoNow's records show Deerfield Imaging, Inc. has 8 other recalls on record since Feb. 20, 2018. Other recent recalls of similar products include IMRIS ORT300 Operating Room Table Recall (Aug. 6, 2026), IMRIS ORT200 Operating Room Table Recall (Aug. 6, 2026), and Philips Azurion 3 M15 System Recall (Jan. 26, 2026).

How to tell if you have this one

Check the part numbers: 114093-000 or 114093-600. For part number 114093-000, look for serial numbers starting with 10005695, 10002998, etc. For part number 114093-600, look for serial numbers starting with 10007411, 10002996, etc.

  • Brand
    Deerfield Imaging
  • Category
    Medical device
FDA recall event · 4 products

All 4 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, China, Australia, Sweden, Germany
Recall numberProduct, codes & lotsQuantity
Z-1263-2018IMRIS ORT100 Table, Part Numbers: (a) 110470-000 (b) 110470-600; (a) 110470-000, Serial Numbers: 10002845, 10002341, 10003629, 10003801, 10002654, 10002795, 10002796, 10002847, 10003830, 10003243, 10003241, 10002607, 10002848, 10005651, 10007348, 10007424, 10004250, 10004439, 10004576, 10006438, 100030007, 10006887, 10006886 (b) 110470-600, Serial Numbers: 10003244, 10003064, 1000306526 units
Z-1264-2018IMRIS ORT200, Removable Operating Room Table, Part Numbers: (a) 113821-000 (b) 113821-600 (c) 114148-000 (d) 114148-600; (a) 113821-000, Serial Numbers: 10006997, 10002220 (b) 113821-600, Serial Numbers: 10002692,10006152, 10007192, 10006991, 10003754, 10006997, 10004513 (c) 114148-000, Serial Numbers: 10004463, 10005189, 10005190, 10006891, 10004997, 10004327 (d) 114148-600, Serial Numbers: 10005201, 1000689117 units
Z-1265-2018IMRIS T2X Table, Part Numbers: (a) 108000-000 (b) 108000-600 (c) 109682-000 (d) 109682-600; (a) 108000-000, Serial Numbers: 10000239, 10000983, 10000233 (b) 108000-600, Serial Numbers: 10001306 (c) 109682-000, Serial Numbers: 10002375, 10001118, 10001340 (d) 109682-600, Serial Numbers: 10001119, 10003623, 05-002, 10003634, 10001188, 10003638, 1000119214 units
Z-1266-2018IMRIS ORT300, Removable Operating Room Table, Part Numbers: (a) 114093-000 (b) 114093-600; (a) 114093-000, Serial Numbers: 10005695, 10002998, 10005456, 10007377, 10002997, 10005612, 10004372, 10002841, 10002255, 10005613 (b) 114093-600, Serial Numbers: 10007411, 10002996, 1000451513 units
Based on the official FDA remedy

What to do — step by step

  1. Contact Manufacturer

    Reach out to Deerfield Imaging for specific instructions on how to handle the recalled tables.

How this recall unfolded

Recall timeline

FDA terminated this recall 19 months after the firm started it.

1. Firm started the recall: Feb 23, 201812. FDA classified it Class II: Mar 28, 201823. Published in FDA’s Enforcement Report: Apr 4, 201834. FDA terminated the recall: Sep 12, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

How can I check if my table is affected?

Check the part numbers and serial numbers against the list provided in the recall notice.

Similar recalls

Safeguard US Recalls Battle Bandages and IFAK Kits Due to Infection Risk
Safeguard US Operating LLCMiniMed Flex Insulin Pump Recall: Inaccurate Delivery Risk
Medtronic MiniMed, Inc.Medline Bariatric Rollator Recall: Detaching Wheels Risk
Medline Industries, LPCooperVision Pearle Vision 1 Day Contact Lenses: Incorrect Power Risk
CooperVision, Inc.Tandem t:slim App Recall: Pairing Issue With Abbott Sensors
Tandem Diabetes Care, Inc.

Latest medical device recalls

BMC Medical Co., Ltd. recalls BMC/REACTHEALTH Luna G3 APAP REF LG 3600
BMC Medical Co., Ltd. · July 15, 2026Medtronic MiniMed, Inc. recalls MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Medtr: MiniMed · July 13, 2026INTEGRATED MEDCRAFT LLC recalls Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway
Medcraft · July 7, 2026Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: R-TRAK Model/Catalog Number: R-TRAK Software Version: 2.0.11, new version:
Quantum Rehab · June 25, 2026ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory
ResMed · June 25, 2026Therabody, Inc recalls Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO
Therabody · June 23, 2026

Keep exploring

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-1266-2018 (February 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1266-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on August 27, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA