Deerfield Imaging ORT200 Operating Room Table Recall: Locking Mechanism Failure
Deerfield Imaging recalls ORT200 operating room tables with serial numbers listed. The rotational locking mechanism may fail to lock, causing unintended movement during procedures.
Use caution until it’s fixed
The rotational locking mechanisms on the ORT 200/300 tables fail to operate such that it cannot change states between locked and unlocked.
Contact the company
What happened, in plain English
Deerfield Imaging recalls certain ORT200 operating room tables due to a failure in the rotational locking mechanism. This could lead to unintended table movement during medical procedures, potentially causing injury. Read more at govinfonow.com/recall/71887-deerfield-imaging-ort200-operating-room-table-recall-locking-mechanism-failure.
Source Summary by GovInfoNow · govinfonow.com/recall/71887-deerfield-imaging-ort200-operating-room-table-recall-locking-mechanism-failure · Updated August 27, 2026 · FDA enforcement record: FDA #Z-1217-2018
Cite this page
“Deerfield Imaging ORT200 Operating Room Table Recall: Locking Mechanism Failure.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/71887-deerfield-imaging-ort200-operating-room-table-recall-locking-mechanism-failure. Based on FDA recall #Z-1217-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1217-2018%22&limit=1).
Why it’s dangerous
The rotational locking mechanism may fail to lock properly, causing the table to move unexpectedly during use. This could lead to patient or staff injury if the table shifts while being positioned or adjusted.
Who’s affected
Healthcare professionals using the ORT200 tables for surgical procedures or diagnostic exams are most at risk. Patients and staff may be affected if the table moves unexpectedly.
How to tell if you have this one
Check for serial numbers listed in the recall: 10006997, 10002692, 10006152, 10007192, 10006991, 10002220, 10003754, 10006997, 10004513, 10005201, 10006891, 10004463, 10005189, 10005190, 10004327, 10004997, 10006891.
- Brand
Deerfield Imaging- Category
Medical device
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, China, Sweden, Germany, Japan, Qatar, France, Audtralia
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1217-2018 | IMRIS ORT200 Removable Operating Room Table, 50-60 Hz Version is intended for use during diagnostic examinations or surgical procedures to support and position a patient.; Serial numbers: 10006997, 10002692, 10006152, 10007192, 10006991, 10002220, 10003754, 10006997, 10004513, 10005201, 10006891, 10004463, 10005189, 10005190, 10004327, 10004997, 10006891 | 17 units |
| Z-1218-2018 | IMRIS ORT300 Removable Operating Room Table, 50-60 Hz Version is intended for use during diagnostic examinations or surgical procedures to support and position a patient.; Serial numbers: 10005695, 10002998, 10005456, 10007411, 10007377, 10002997, 10002996, 10005612, 10004372, 10002841, 10004515, 10005613, 10002255 | 13 units |
What to do — step by step
Check Table Serial Number
Look for the serial numbers listed in the recall: 10006997, 10002692, 10006152, 10007192, 10006991, 10002220, 10003754, 10006997, 10004513, 10005201, 10006891, 10004463, 10005189, 10005190, 10004327, 10004997, 10006891.
How this recall unfolded
Recall timeline
FDA terminated this recall 18 months 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.
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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-1217-2018 (February 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1217-2018 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.