Device recall
Z-1411-2019: OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01…
FDA device recall · Class II · Oakworks Inc
Key facts
| Recall number (Z-number) | Z-1411-2019 |
|---|---|
| Recall event | 82852 |
| Product | OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks Imaging Tables are radiographic tables intended for use with mobile or compact stationary C-arm Imaging Systems. It is ideally suited for pain management imaging and therapeutic procedures. These… |
| Product code | IXR |
| Recalling firm | Oakworks Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 8, 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