Oakworks Lithotripsy/Urology Table Recall: Incorrect Actuators Risk Injury
Oakworks recalls specific lithotripsy/urology tables with assembly errors that could cause injury during use. Affected models include CFLU401 with serial numbers FLL745088-90. Contact Oakworks for details.
Use caution until it’s fixed
Table assembly error with incorrect actuators for the lateral and longitudinal table movements
Contact the company
What happened, in plain English
Oakworks is recalling certain lithotripsy and urology imaging tables due to a manufacturing error that could cause injury during use. These tables have incorrect actuators for table movements, which may lead to unsafe positioning of patients or equipment. Read more at govinfonow.com/recall/67967-oakworks-lithotripsy-urology-table-recall-incorrect-actuators-risk-injury.
Source Summary by GovInfoNow · govinfonow.com/recall/67967-oakworks-lithotripsy-urology-table-recall-incorrect-actuators-risk-injury · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1411-2019
Cite this page
“Oakworks Lithotripsy/Urology Table Recall: Incorrect Actuators Risk Injury.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/67967-oakworks-lithotripsy-urology-table-recall-incorrect-actuators-risk-injury. Based on FDA recall #Z-1411-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1411-2019%22&limit=1).
Why it’s dangerous
The table has incorrect actuators for lateral and longitudinal movements, which could cause improper positioning of the patient or equipment during procedures. This might lead to injury if the table moves unexpectedly or fails to stabilize during use.
Who’s affected
Healthcare professionals using Oakworks lithotripsy/urology tables with serial numbers FLL745088, FLL745089, or FLL745090 are most at risk. These tables are used in medical settings for procedures like spinal injections and vertebroplasty.
How to tell if you have this one
Check for serial numbers FLL745088, FLL745089, or FLL745090 on the table. These specific models were sold with the catalog number 75216-T01 and are used for lithotripsy and urology procedures.
- Brand
Oakworks- Category
Medical device
What to do — step by step
Check Table Serial Number
Look for serial numbers FLL745088, FLL745089, or FLL745090 on the table to confirm if it is affected.
Contact Oakworks
Reach out to Oakworks directly for further instructions on how to address the issue.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution in the state of SC.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2 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-1411-2019 (May 2, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1411-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 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.