{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Uppsala",
      "state": "",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74801",
      "recalling_firm": "Novus Scientific Ab",
      "address_1": "Virdings Alle 2",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US : IL, CA, FL, KY, MO, NH, VA, TX, NC, OH, NY, TN,   Worldwide:  Sweden, Italy, Denmark, UK, Singapore, Germany, Belgium, Spain, Austria, Israel, Malta, Switzerland, Ireland, Norway, Netherlands, Turkey, New Zealand, Bulgaria, France, Iran, Finland, Poland, South Africa",
      "recall_number": "Z-2603-2016",
      "product_description": "TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030",
      "product_quantity": "3458 units total (657 units in US)",
      "reason_for_recall": "Novus Scientific is implementing additions to the product's instructions for use concerning certain inguinal hernia repairs.",
      "recall_initiation_date": "20160719",
      "center_classification_date": "20160819",
      "termination_date": "20161223",
      "report_date": "20160831",
      "code_info": "",
      "more_code_info": ""
    }
  ]
}