{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Largo",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63823",
      "recalling_firm": "Linvatec Corp. dba ConMed Linvatec",
      "address_1": "11311 Concept Blvd",
      "address_2": "N/A",
      "postal_code": "33773-4908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including California and Internationally to Spain and Korea",
      "recall_number": "Z-0789-2013",
      "product_description": "ConMed Linvatec Biomaterials, PopLok bone Punch   PKL-35M, 3.5mm      Orthopedic manual surgical instrument - Bone Punch",
      "product_quantity": "8",
      "reason_for_recall": "ConMed Linvatech recalled one lot of their PopLok bone Punch 3.5mm because the metal shaft diameter is 4.5mm when it should be 3.5mm.",
      "recall_initiation_date": "20121115",
      "center_classification_date": "20130205",
      "termination_date": "20130522",
      "report_date": "20130213",
      "code_info": "Lot 256058",
      "more_code_info": ""
    }
  ]
}