FDA Device recall Z-2208-2015
Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position
- FDA Device
- Class II
- terminated
- Published 2015-07-29
On 2015-07-29 the FDA classified a Class II recall of Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position by Silhouette Lift, citing silhouette Lift is recalling the Silhouette Suture brochure because it does not include a complete list of risks and side effects. Therefore, it can potentially mislead the patien….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2208-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-02 |
| Published | 2015-07-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Silhouette Lift |
| Distribution | CA, CO, FL, GA, IA, MA, MI, MO, NE, NY, PA, RI, TX, VA, WI |
Product
Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position.
Reason
Silhouette Lift is recalling the Silhouette Suture brochure because it does not include a complete list of risks and side effects. Therefore, it can potentially mislead the patient regarding the safety of the product.
Identifiers
| code_info | n/a. This action does not involve recall or correction of any device. Only marketing materials are being considered in this action |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2208-2015%22
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