{
  "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": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71121",
      "recalling_firm": "Medacta Usa",
      "address_1": "1556 W Carroll Ave",
      "address_2": "N/A",
      "postal_code": "60607-1012",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of IL, OH and UT, and the countries of in Austria, Spain, Australia, France and Switzerland.",
      "recall_number": "Z-0275-2016",
      "product_description": "GMK Hinge knee prosthesis; Model Number: 02.09.TA410; Orthopedics and Orthopedic Surgery",
      "product_quantity": "4 units (US)",
      "reason_for_recall": "Incorrect parts: Packages of the GMK Hinge Tibial Augmentation size 4-10 mm have 5 mm screws instead of 10 mm screws.",
      "recall_initiation_date": "20150417",
      "center_classification_date": "20151113",
      "termination_date": "20170105",
      "report_date": "20151125",
      "code_info": "Lot: 145129"
    }
  ]
}