{
  "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": "A single lot of product that potentially has a single part within the lot that does not match the product on the label due to a commingle at the firm supplier",
      "address_2": "",
      "product_quantity": "5",
      "code_info": "LTX610, lot 1199571; UDI: (01)00844868009917(17)210916(10)1199571",
      "center_classification_date": "20170329",
      "distribution_pattern": "Argentina",
      "state": "FL",
      "product_description": "BIOMET  3i LTX DENTAL IMPLANTS   Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardboard box; one (1) unit per box.  Labeled \u001cSterile\"",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet 3i, LLC",
      "recall_number": "Z-1701-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76809",
      "termination_date": "20190802",
      "more_code_info": "",
      "recall_initiation_date": "20170308",
      "postal_code": "33410-4200",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}