{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Malden",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83166",
      "recalling_firm": "SpineFrontier, Inc.",
      "address_1": "350 Main St",
      "address_2": "N/A",
      "postal_code": "02148-5089",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  AZ, MD, MO, and FL.",
      "recall_number": "Z-1973-2019",
      "product_description": "A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)",
      "product_quantity": "6",
      "reason_for_recall": "There is a potential for the driver to bind up when attempting to advance the intervertebral body fixation screw.",
      "recall_initiation_date": "20190613",
      "center_classification_date": "20190712",
      "termination_date": "20200511",
      "report_date": "20190724",
      "code_info": "Lot EC20"
    }
  ]
}