{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Memphis",
      "address_1": "6060 Poplar Ave Ste 380",
      "reason_for_recall": "The NeoSpan Compression Staple (10x10x10) kits from two lots contain the wrong size drill bit.  They contain a 3mm drill bit instead of a 2mm drill bit.",
      "address_2": "",
      "product_quantity": "30 units",
      "code_info": "Lot Number:  9G88C0",
      "center_classification_date": "20181222",
      "distribution_pattern": "TX, VA, PA, MO, NJ, FL, TN, NC, OH, WI, LA",
      "state": "TN",
      "product_description": "NeoSpan SuperElastic Compression Staple w/Instruments, Size 10x10x10, Part Number T50 SN010",
      "report_date": "20190102",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "In2bones USA, LLC",
      "recall_number": "Z-0670-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81655",
      "termination_date": "20190508",
      "more_code_info": "",
      "recall_initiation_date": "20181114",
      "postal_code": "38119-3915",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}