Device recall
Z-0703-2018: Foot Controls impacted for the following devices: OAKWORKS Medical CFPM 300…
FDA device recall · Class II · Oakworks Inc
Key facts
| Recall number (Z-number) | Z-0703-2018 |
|---|---|
| Recall event | 79107 |
| 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… |
| Product code | IXR |
| Recalling firm | Oakworks Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 29, 2019 |
| FEI number | 1000121370 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database