{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Largo",
      "address_1": "11311 Concept Blvd",
      "reason_for_recall": "ConMed Linvatec recalled one lot of their PopLok bone Punch 3.5MM because the metal shaft diameter is 4.5mm when it should have been 3.5mm.",
      "address_2": "",
      "product_quantity": "2",
      "code_info": "Lot 318455",
      "center_classification_date": "20120806",
      "distribution_pattern": "Worldwide Distribution -- US and Korea.",
      "state": "FL",
      "product_description": "PopLok Punch labeled in part:  \"PKL-35M***3.5mm***QTY 1***PopLok Punch***ConMed Linvatec Biomaterials, Ltd. Hermiankatu 6-8L 33720 Tampere, FINLAND***Rx Only***ConMed Linvatec 11311 Concept Blvd Largo, FL 33773-4908 USA***Made in USA***\"    Intended Use:  Bone Punch.",
      "report_date": "20120815",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Linvatec Corp. dba ConMed Linvatec",
      "recall_number": "Z-2151-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62665",
      "termination_date": "20131121",
      "more_code_info": "",
      "recall_initiation_date": "20120706",
      "postal_code": "33773-4908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}