🔍 RecallPedia

Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position.

Class I - Dangerous
🏥 Medical Devices Recalled: July 2, 2015 Silhouette Lift Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    n/a. This action does not involve recall or correction of any device. Only marketing materials are being considered in this action
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Silhouette Lift, Inc.
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position.

Product Codes/Lot Numbers:

n/a. This action does not involve recall or correction of any device. Only marketing materials are being considered in this action

Distribution:

Distributed in: US, CA, TX, IA, MA, RI, GA, WI, PA, VA, MO, FL, NE, MI, NY, CO

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2208-2015