Device recall
Z-1818-2008: ClearView Uterine Manipulator with disposable Sound-Dilator (DSD-1000), REF…
FDA device recall · Class II · Clinical Innovations, LLC
Key facts
| Recall number (Z-number) | Z-1818-2008 |
|---|---|
| Recall event | 48115 |
| Product | ClearView Uterine Manipulator with disposable Sound-Dilator (DSD-1000), REF UM210, 7 cm, Sterile, Clinical Innovations, 747 West 4170 South, Murray, Utah 84123. |
| Product code | LKF |
| Recalling firm | Clinical Innovations, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 25, 2008 |
| 510(k) numbers | K940681 |
| FEI number | 1000220650 |
At a glance
- 1–9 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