{
  "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": [
    {
      "country": "United States",
      "city": "Palm Beach Gardens",
      "address_1": "4555 Riverside Dr",
      "reason_for_recall": "Product was incorrectly packaged.",
      "address_2": "",
      "product_quantity": "92 units",
      "code_info": "Model No: IOSS411; Lot No: 2016031461; UDI: (01)00844868007098(17)210401(10)2016031461.",
      "center_classification_date": "20160919",
      "distribution_pattern": "US Distributions to the states of : CA and FL., and Worldwide to : Colombia, France, Germany, Italy, and Spain.",
      "state": "FL",
      "product_description": "3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet 3i, LLC",
      "recall_number": "Z-2845-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74896",
      "termination_date": "20190806",
      "more_code_info": "",
      "recall_initiation_date": "20160808",
      "postal_code": "33410-4200",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}