Oakworks Medical Foot Controls Recall: Foot Controls May Get Stuck Under Table
Oakworks recalls medical imaging tables with foot controls that can become lodged under the table base or column, posing a risk of injury during use. Affected models include CFPM 300, CFPM 301, and others. Consumers should check their table model and contact Oakworks for details.
Use caution until it’s fixed
The foot control used on the OAKWORKS¿ Inc., CFPM300, CFPM301, CFPM400, CFPM401, CFPMB301, CFUR301, CFUR401 and CFLU401 Imaging Tables can become lodged under the base or under the column of the table.
Contact the company
What happened, in plain English
Oakworks is recalling medical imaging tables with foot controls that can become lodged under the table base or column. This could cause the table to move unexpectedly, potentially leading to injury during medical procedures. Read more at govinfonow.com/recall/73297-oakworks-medical-foot-controls-recall-foot-controls-may-get-stuck.
Source Summary by GovInfoNow · govinfonow.com/recall/73297-oakworks-medical-foot-controls-recall-foot-controls-may-get-stuck · Updated September 20, 2026 · FDA enforcement record: FDA #Z-0703-2018
Cite this page
“Oakworks Medical Foot Controls Recall: Foot Controls May Get Stuck Under Table.” GovInfoNow, updated September 20, 2026. https://govinfonow.com/recall/73297-oakworks-medical-foot-controls-recall-foot-controls-may-get-stuck. Based on FDA recall #Z-0703-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0703-2018%22&limit=1).
Why it’s dangerous
The foot control can become lodged under the table base or column, causing the table to shift or move unexpectedly during use. This could lead to injury to patients or staff if the table moves suddenly while being adjusted.
Who’s affected
Medical facilities using Oakworks imaging tables with specific model numbers, such as CFPM 300, CFPM 301, CFPM 400, and others, are most at risk. Patients and staff during procedures may be affected if the table moves unexpectedly.
How to tell if you have this one
Check if your imaging table has a model number starting with CFPM 300, CFPM 301, CFPM 400, CFPM 401, CFPMB 301, CFUR 301, CFUR 401, or CFLU 401. The catalog numbers listed in the recall notice also indicate affected units.
- Brand
Oakworks- Category
Medical device
What to do — step by step
Check Table Model
Identify your imaging table's model number to see if it matches the recalled models listed in the recall notice.
Contact Oakworks
Reach out to Oakworks directly for further instructions on how to address the issue with your specific table model.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “USA (nationwide) Distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 20 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.
Questions people ask
How can I tell if my table has the faulty foot control?
Check your table's model number against the list of affected models provided in the recall notice.
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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-0703-2018 (July 31, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0703-2018 to see it in context.
- Plain-language summary written by qwen3:4b on September 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.