Deerfield Imaging IMRIS T2X Table Recall: Risk of Drifting During Use
Deerfield Imaging recalls IMRIS T2X tables with specific part numbers due to potential drifting in roll position during use. Affected models may require correction to prevent patient positioning issues.
Use caution until it’s fixed
Table may drift in the roll position while in use
Contact the company
What happened, in plain English
Deerfield Imaging is recalling IMRIS T2X medical tables with specific part numbers because they may drift in roll position while in use. This could lead to improper patient positioning during medical procedures. Read more at govinfonow.com/recall/69494-deerfield-imaging-imris-t2x-table-recall-risk-of-drifting-during.
Source Summary by GovInfoNow · govinfonow.com/recall/69494-deerfield-imaging-imris-t2x-table-recall-risk-of-drifting-during · Updated August 20, 2026 · FDA enforcement record: FDA #Z-0645-2019
Cite this page
“Deerfield Imaging IMRIS T2X Table Recall: Risk of Drifting During Use.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/69494-deerfield-imaging-imris-t2x-table-recall-risk-of-drifting-during. Based on FDA recall #Z-0645-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0645-2019%22&limit=1).
Why it’s dangerous
The table may shift in roll position during use, which could cause improper patient positioning. This might lead to complications during medical procedures like imaging or surgery.
Who’s affected
Medical facilities using the IMRIS T2X tables with the listed part numbers are most at risk. Patients undergoing imaging or surgical procedures on these tables could be affected if the table drifts.
How to tell if you have this one
Check the part numbers listed: (a)108000-000, (b)108000-600, (c)109682-000, (d)109682-600, or (e)110470-600. The tables are used in medical settings for imaging and surgical procedures.
- Brand
Deerfield Imaging- Category
Medical device
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
Worldwide distribution - US Nationwide and countries of China, Qatar, Canada, Australia, Japan, France, Germany, Sweden, Italy.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-0645-2019 | IMRIS T2X table, Part Numbers: (a)108000-000, (b)108000-600, (c)109682-000, (d) 109682-600, (e) 110470-600 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a patient. The tables are indicated for imagining from head to sacrum with MR/CT imaging modalities. The ORT100 table is intended for use during diagnostic examination or surgical procedures to support and position the patient.; (a)108000-000, Serial Numbers: 10000983, 10000652 (b)108000-600, Serial Numbers: 06-0025, 10001306 (c)109682-000, Serial Numbers: 10002375, 10001118, 10001340 (d)109682-600, Serial Numbers: 10001119, 10001188, 10003634, 05-002, 10003638, 10003623, 10001305 (e)110470-600, Serial Numbers: 10006887 | 15 units |
| Z-0646-2019 | IMRIS ORT 100 table, Part Numbers: (a) 110470-000, (b) 110470-600 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a patient. The tables are indicated for imagining from head to sacrum with MR/CT imaging modalities. The ORT100 table is intended for use during diagnostic examination or surgical procedures to support and position the patient.; (a) 110470-000, Serial Numbers: 10002845, 10002341, 10003629, 10003801, 10003830, 10002847, 10002796, 10003243, 10002654, 10003841, 10002607, 10007348, 10007424, 10005651, 10004250, 10004439, 10003241, 10006886, 10002848, 10006438, 10003007, 10004576, 10003245 (b) 110470-600, Serial Numbers: 10003244, 10003064, 10003244, 10002343 | 27 units |
| Z-0647-2019 | IMRIS ORT 200, Removable Operating Room Table, Part Numbers: (a) 113821-000, (b) 113821-600, (c) 114148-000, (d) 114148-600 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a patient. The tables are indicated for imagining from head to sacrum with MR/CT imaging modalities. The ORT100 table is intended for use during diagnostic examination or surgical procedures to support and position the patient.; (a) 113821-000, Serial Numbers: 10002220 (b) 113821-600, Serial Numbers: 10002692, 10006152, 10007192, 10006991, 10003754, 10006997, 10004513 (c) 114148-000, Serial Numbers: 10004463, 10005190, 10005189, 10006891, 10004997 (d) 114148-600, Serial Numbers: 10006891 | 14 units |
| Z-0648-2019 | IMRIS ORT 300, Removable Operating Room Table, Part Numbers: (a) 114093-000, (b) 114093-006 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a patient. The tables are indicated for imagining from head to sacrum with MR/CT imaging modalities. The ORT100 table is intended for use during diagnostic examination or surgical procedures to support and position the patient.; (a) 114093-000, Serial Numbers: 10005695, 10002998, 10005456, 10007377, 10002997, 10005612, 10004372, 10002841 10002255, 10002385, 10005613 (b) 114093-006, Serial Numbers: 10007411, 10002996, 10004515 | 14 units |
What to do — step by step
Check Part Numbers
Identify if your table has part numbers (a)108000-000, (b)108000-600, (c)109682-000, (d)109682-600, or (e)110470-600.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide and countries of China, Qatar, Canada, Australia, Japan, France, Germany, Sweden, Italy.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 2.7 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using this table immediately?
No, but you should check if your table has the affected part numbers and take corrective action if needed.
Similar recalls
Latest medical device recalls
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-0645-2019 (November 6, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0645-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 20, 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.