{
  "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": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68565",
      "recalling_firm": "Smith & Nephew, Inc. Endoscopy Division",
      "address_1": "150 Minuteman Drive",
      "address_2": "N/A",
      "postal_code": "01810-1031",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Australia, Belgium, Denmark, France, Germany, Great Britain, Italy, Netherlands, Norway, Portugal, Spain, and Sweden.",
      "recall_number": "Z-2049-2014",
      "product_description": "SUTUREFIX Ultra S Double Loaded Suture  Product Code: 72203854    Fastener, fixation, nondegradable, soft tissue",
      "product_quantity": "763 units",
      "reason_for_recall": "Sterility of device is compromised due to breach in sterile barrier",
      "recall_initiation_date": "20140602",
      "center_classification_date": "20140714",
      "termination_date": "20170915",
      "report_date": "20140723",
      "code_info": "Lot Numbers: 50478984,50485736, 50485737, 50485738, 50487831,  50491901, 50493684"
    }
  ]
}