{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Beverly",
      "address_1": "500 Cummings Ctr Ste 3500",
      "reason_for_recall": "The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle Screw System may be used incorrectly as the Surgical Technique does not adequately convey the intended use of the design.",
      "address_2": "",
      "product_quantity": "5 devices",
      "code_info": "Revision E",
      "center_classification_date": "20150421",
      "distribution_pattern": "US Nationwide Distribution in the states of  TX, KS, CO, and MA",
      "state": "MA",
      "product_description": "SpineFrontier  MISquito  Percutaneous Pedicle Screw System Surgical Technique; Part Number: DOC80023.   The Rod Caliper is a manual surgical instrument that may be used as part of the PedFuse Pedicle Screw System and its MISquito components during percutaneous, minimally invasive surgical (MIS) technique of posterior pedicle screw fixation.",
      "report_date": "20150429",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "SpineFrontier, Inc.",
      "recall_number": "Z-1479-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "70488",
      "termination_date": "20150615",
      "more_code_info": "",
      "recall_initiation_date": "20150305",
      "postal_code": "01915-6516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}