{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86923",
      "recalling_firm": "Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the state of FL and the countries of Korea, Japan, Netherlands.",
      "recall_number": "Z-0723-2021",
      "product_description": "Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty    Item Number: 185422",
      "product_quantity": "21 units",
      "reason_for_recall": "Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure",
      "recall_initiation_date": "20201201",
      "center_classification_date": "20201223",
      "termination_date": "20220708",
      "report_date": "20201230",
      "code_info": "Lot Number: 098780    UDI Number: (01) 00880304482739 (17) 290501 (10) 098780"
    }
  ]
}