Device recall
Z-2208-2015: Silhouette Lift brochure Silhouette Sutures are for use in midface suspension…
FDA device recall · Class II · Silhouette Lift, Inc.
Key facts
| Recall number (Z-number) | Z-2208-2015 |
|---|---|
| Recall event | 71615 |
| Product | Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position. |
| Product code | GAM |
| Recalling firm | Silhouette Lift, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2016 |
| 510(k) numbers | K060414 |
| FEI number | 3007009755 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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