# FDA recall Z-0703-2018

> **Oakworks Inc** · Class II · device recall initiated 2017-07-31.

## 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

## Reason for recall

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.

## Distribution

USA (nationwide) Distribution

## Key facts

- **Recall number:** Z-0703-2018
- **Recalling firm:** Oakworks Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-31
- **Report date:** 2018-03-07
- **Termination date:** 2019-03-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New Freedom, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0703-2018

## Citation

> AI Analytics. FDA recall Z-0703-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0703-2018. Source: US FDA. Licensed CC0.

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