{
  "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": "Beverly",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64991",
      "recalling_firm": "SpineFrontier, Inc.",
      "address_1": "500 Cummings Ctr Ste 3500",
      "address_2": "N/A",
      "postal_code": "01915-6516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "Worldwide distribution: US (nationwide) to states of: CO, MA, and TX; and country of: Jamaica.",
      "recall_number": "Z-1482-2013",
      "product_description": "Straight Impactor - Dorado IBC, Part Number: SI02140. The device is used to position implants after they have been inserted into the disc space during implantation of intervertebral body fusion devices.",
      "product_quantity": "10",
      "reason_for_recall": "During two separate occasions an impactor plate on the handle broke off while being struck by a mallet.",
      "recall_initiation_date": "20080510",
      "center_classification_date": "20130605",
      "termination_date": "20141008",
      "report_date": "20130612",
      "code_info": "Lot number:  20856"
    }
  ]
}