{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71615",
      "recalling_firm": "Silhouette Lift, Inc.",
      "address_1": "1 Technology Dr Ste F211",
      "address_2": "N/A",
      "postal_code": "92618-5336",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : CA, TX, IA, MA, RI, GA, WI, PA, VA, MO, FL, NE, MI, NY and CO., and Internationally to Canada.",
      "recall_number": "Z-2208-2015",
      "product_description": "Silhouette Lift brochure    Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position.",
      "product_quantity": "2,260 units",
      "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.",
      "recall_initiation_date": "20150702",
      "center_classification_date": "20150723",
      "termination_date": "20160205",
      "report_date": "20150729",
      "code_info": "n/a.    This action does not involve recall or correction of any device. Only marketing materials are being considered in this action"
    }
  ]
}