{
  "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": [
    {
      "status": "Terminated",
      "city": "Largo",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63090",
      "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": "E-Mail",
      "distribution_pattern": "Worldwide Distribution--US (nationwide) including state of Minnesota and the country of Thailand",
      "recall_number": "Z-0164-2013",
      "product_description": "\"***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA***\"    To create pathway for insertion of CrossFT Suture Anchor into bone.",
      "product_quantity": "2 units",
      "reason_for_recall": "ConMed Linvatec is recalling the product due to the punch being mis-assembled with the incorrect handled.  The correct handle is a clear anodized silver colored handle.",
      "recall_initiation_date": "20120409",
      "center_classification_date": "20121029",
      "termination_date": "20131121",
      "report_date": "20121107",
      "code_info": "Lot # 330889 and Catalog: PFT-00M - No Expiration date",
      "more_code_info": ""
    }
  ]
}