{
  "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": "64669",
      "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": "Nationwide Distribution including CA, FL, GA, MA, MI, NC, SC, OH, and MO.",
      "recall_number": "Z-1132-2013",
      "product_description": "TRIGEN (TM) L-P SCREW, 4.5 MM X 37.5 MM, TI-6AL-4V, QTY: (1), STERILE R, REF 71645437, Smith & Nephew, Inc. Memphis, TN 38116 USA    orthopedic surgery",
      "product_quantity": "23 units",
      "reason_for_recall": "One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly anodized with a gold coating (indicating a 5 mm diameter) instead of a gray coating (indicating a 4.5 mm diameter).",
      "recall_initiation_date": "20130306",
      "center_classification_date": "20130417",
      "termination_date": "20190816",
      "report_date": "20130424",
      "code_info": "Lot Number 12FM12182"
    }
  ]
}