{
  "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": "Bloomington",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71913",
      "recalling_firm": "Tornier, Inc",
      "address_1": "10801 Nesbitt Ave S",
      "address_2": "N/A",
      "postal_code": "55437-3109",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to CA, ME, NC, PA, and TX.",
      "recall_number": "Z-2465-2015",
      "product_description": "Salto Talaris Tibial Guide, Part # MJU333 ,Tray/Kit Code YKAL11,  Non sterile.    Orthopedic Manual Surgical Instrument",
      "product_quantity": "5",
      "reason_for_recall": "Tornier has initiated a voluntary recall for the Salto Talaris Tibial Guide (part number MJU333) due to a  complaint that occurred during physician training, that the guide cannot be assembled to the Salto Talaris Talar Pin Setting guide. This issue will cause the impossibility  the time of putting the Talar pin in the guide.",
      "recall_initiation_date": "20150806",
      "center_classification_date": "20150826",
      "termination_date": "20160408",
      "report_date": "20150902",
      "code_info": "Lot #14F005"
    }
  ]
}