Class II — Oakworks Inc
| Recalling firm | Oakworks, INC. |
|---|---|
| Registered facility | OAKWORKS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| Product | Foot Controls impacted for the following devices: OAKWORKS® Medical CFPM 300 Imaging Table OAKWORKS® Medical CFPM 301 Imaging Table OAKWORKS® Medical CFPM 400 Imaging Table OAKWORKS® Medical CFPM 401 Imaging Table OAKWORKS® Medical CFPMB 301 Bariatric Imaging Table OAKWORKS® Medical CFUR 301 Urology Table OAKWORKS® Medical CFUR 401 Urology Table OAKWORKS® Medical CFLU 401 Lithotripsy/Urology Table |
| Quantity | 1,104 |
| Distribution | USA (nationwide) Distribution |
| Initiated | 2017-07-31 |
| Classified | 2018-02-23 |
| Terminated | 2019-03-29 |
| Recall number | Z-0703-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Oakworks Inc (Z-0703-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/79107/
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