{
  "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": "Largo",
      "address_1": "11311 Concept Blvd",
      "reason_for_recall": "ConMed Linvatec recalled lot number #156920, PFT-45M, CrossFT Punch because there is a possibility that the device was etched incorrectly listing the item number as PFT-00M and includes incorrect depth lines for insertion.",
      "address_2": "",
      "product_quantity": "2",
      "code_info": "Lot  #156920",
      "center_classification_date": "20120806",
      "distribution_pattern": "Nationwide Distribution, including the states of Colorado and Pennsylvania.",
      "state": "FL",
      "product_description": "CrossFT Punch, Product Number PFT-45M.  Manufacturer: CONMED LINVATEC.  The intended use is to create a hole to facilitate insertion of the CrossFT suture anchor into bone.",
      "report_date": "20120815",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Linvatec Corp. dba ConMed Linvatec",
      "recall_number": "Z-2147-2012",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "62395",
      "termination_date": "20131121",
      "more_code_info": "",
      "recall_initiation_date": "20110812",
      "postal_code": "33773-4908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}