{
  "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": "A crack may develop in the handle to the Inline Persuader, which may progress if the user continues to use the affected instrument.",
      "address_2": "",
      "product_quantity": "4 devices",
      "code_info": "Lot/Serial Numbers: 06440-0000, 06441-0000, AG24",
      "center_classification_date": "20150114",
      "distribution_pattern": "Nationwide Distribution including TX, OH, VA, and Washington, DC.",
      "state": "MA",
      "product_description": "lnline Persuader- PedFuse Pedicle Screw System; Part Number:  11-80164",
      "report_date": "20150121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "SpineFrontier, Inc.",
      "recall_number": "Z-0977-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "70065",
      "termination_date": "20160111",
      "more_code_info": "",
      "recall_initiation_date": "20141219",
      "postal_code": "01915-6516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}