{
  "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": "Marquette",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68619",
      "recalling_firm": "PIONEER SURGICAL TECHNOLOGY, INC.",
      "address_1": "375 River Park Cir",
      "address_2": "N/A",
      "postal_code": "49855-1781",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution in the states of TX and FL",
      "recall_number": "Z-2076-2014",
      "product_description": "Tritium Sternal Plate System, Screw, 02.7mm X 12mm, 12 Pack, Sterile.       The Pioneer Surgical Cable Plate System is used in the stabilization and fixation of fractures of the anterior chest wall including Sternal fixation following Sternotomy and Sternal reconstructive surgical procedures.   The screws are packaged as a 12 pack using a double tray packaging configuration.",
      "product_quantity": "5",
      "reason_for_recall": "Lack of Sterility Assurance",
      "recall_initiation_date": "20140611",
      "center_classification_date": "20140717",
      "termination_date": "20141022",
      "report_date": "20140723",
      "code_info": "Model: 86-27-12-S12  UDI Number: 00846468061463  LOT: 168952  Expiration:12/23/2018"
    }
  ]
}