{
  "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": "72598",
      "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": "Worldwide Distribution - US including CA, CO, NY, OH, WA, AZ MI, MD, GA, NC, and Internationally to Iran.",
      "recall_number": "Z-0391-2016",
      "product_description": "RBT, Internal Implant, Laser-Lok, 5.0 x 15mm, 5.7 Platform, REF LPBR5015, Rx only, Sterile R, BIOHORIZONS(R),   Dental Implant",
      "product_quantity": "32 units",
      "reason_for_recall": "An incorrect label reading \u001c10.5mm\u001d and not the specified \u001c15mm\u001d was placed on the implant inner vial packaging.",
      "recall_initiation_date": "20151030",
      "center_classification_date": "20151207",
      "termination_date": "20160204",
      "report_date": "20151216",
      "code_info": "Lot 1404442",
      "more_code_info": ""
    }
  ]
}