Oakworks, INC.
5 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (5)
Registered facilities (1)
- OAKWORKS, INC. FEI 1000121370 · PA
Recalls & enforcement
- Class IIOngoing2023-12-05Backrest platform stress fracture - the table is not operational in an inclined position
- Class IITerminated2022-04-21The warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.
- Class IITerminated2021-06-29Weld failure- the bracket attaches the tabletop tilting actuator to the tabletop frame. If the bracket weld fails, the tabletop tilting action is non-functional
- Class IITerminated2019-05-02Table assembly error with incorrect actuators for the lateral and longitudinal table movements
- Class IITerminated2017-07-31The 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.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Oakworks, INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9004167-oakworks-inc/
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