{
  "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": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64342",
      "recalling_firm": "Smith & Nephew Inc",
      "address_1": "1450 E. Brooks Rd",
      "address_2": "N/A",
      "postal_code": "38116",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - USA including NM, TN, TX, NC, CA, MI, KY, MA, NJ, OH, and HI.  Internationally to Canada, United Arab Emirates, Mexico, Argentina, Japan, and Chile.",
      "recall_number": "Z-0943-2013",
      "product_description": "INTERNAL HEX RECON SCREW, TI-6AL-4V, REF 7162380, TRIGEN (R) INTERNAL HEX CAPTURED RECON SCREW, QTY: (1), 6.4 MM, 80 MM, TITANIUM, Smith & Nephew, Inc. Orthopedic.  Bone screw for intramedullary rod fixation.",
      "product_quantity": "69 units",
      "reason_for_recall": "75 mm screws were packaged and labeled using an 80 mm screw outer box and label, while 80 mm screws were packaged and labeled using a 75 mm screw outer box and label.",
      "recall_initiation_date": "20130207",
      "center_classification_date": "20130313",
      "termination_date": "20160111",
      "report_date": "20130320",
      "code_info": "Batch Number 12KM01206",
      "more_code_info": ""
    }
  ]
}