{
  "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": "Belgrade",
      "state": "MT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64486",
      "recalling_firm": "Bacterin International, Inc.",
      "address_1": "600 Cruiser Ln",
      "address_2": "N/A",
      "postal_code": "59714-9719",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "USA Nationwide Distribution",
      "recall_number": "Z-1138-2013",
      "product_description": "OsteoSelect  DBM Putty    Product Usage:  Orthopedic bone filler",
      "product_quantity": "165",
      "reason_for_recall": "The firm's retesting procedure was not validated.",
      "recall_initiation_date": "20130221",
      "center_classification_date": "20130417",
      "termination_date": "20130701",
      "report_date": "20130424",
      "code_info": "B100164 and B110115"
    }
  ]
}