{
  "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": [
    {
      "country": "United States",
      "city": "Marquette",
      "address_1": "375 River Park Cir",
      "reason_for_recall": "Some set screw thread profiles were found not to be within specifications.",
      "address_2": "",
      "product_quantity": "11 sets",
      "code_info": "Lot numbers: 104875, 104876, 104877, 104878, 104879, 104880, 104881 , 117030,117031 , 121947, 124260.",
      "center_classification_date": "20140903",
      "distribution_pattern": "Distributed in the states of NC, NH, NY, CA, MI, IL, and FL.",
      "state": "MI",
      "product_description": "STREAMLINE CT CERVICO-THORACIC SYSTEM; SET SCREW  REF 26-SETSCREW  NON-STERILE, SINGLE USE, RX ONLY",
      "report_date": "20140910",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "PIONEER SURGICAL TECHNOLOGY, INC.",
      "recall_number": "Z-2573-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "69033",
      "termination_date": "20140930",
      "more_code_info": "",
      "recall_initiation_date": "20120910",
      "postal_code": "49855-1781",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}