{
  "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": [
    {
      "status": "Terminated",
      "city": "Hoover",
      "state": "AL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71125",
      "recalling_firm": "BioHorizons Implant Systems Inc",
      "address_1": "2300 Riverchase Ctr",
      "address_2": "N/A",
      "postal_code": "35244-2808",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide in the states of:  AL, FL, MS, VA, LA, CA, NC, TX, TN, OH, OK, VT, WA, MD, NY, SD, and SC.",
      "recall_number": "Z-1605-2015",
      "product_description": "Tapered HD Upgrade Set, REF  TSKHDUS, Non-Sterile, Rx Only,     Product Usage  Usage:  Surgical instruments used in preparation for dental implant placement",
      "product_quantity": "48 units",
      "reason_for_recall": "BioHorizons Tapered HD Upgrade set was packaged with an incorrect drill component manufactured of stainless steel in place of the correct component manufactured from titanium.",
      "recall_initiation_date": "20150416",
      "center_classification_date": "20150512",
      "termination_date": "20150807",
      "report_date": "20150520",
      "code_info": "Lot Number 1501968",
      "more_code_info": ""
    }
  ]
}