Product Wiki · Recalls · U.S. FDA — Device Enforcement

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.

U.S. FDA — Device Enforcement · United States · 2015-07-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2208-2015
Date of alert
2015-07-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Silhouette Lift, Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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