{
  "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": "Utica",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63981",
      "recalling_firm": "ConMed Corporation",
      "address_1": "525 French Road",
      "address_2": "N/A",
      "postal_code": "13502",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) Puerto Rico and internationally to Belgium, Colombia, Czech Republic, Dubai, Guatemala, Hong Kong, India, Israel, Italy, Japan, Kenya, Kuwait, Malaysia, Mexico, New Zealand, Norway, Oman, Pakistan, Portugal, Saudi Arabia, Thailand, and Uruguay.",
      "recall_number": "Z-0737-2013",
      "product_description": "UltraClean(R) Accessory Electrode 4 inch Coated Blade with Extended Insulation,  REF/Catalog No. 139112EXT, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION  Electrosurgical, Cutting and Coagulation and Accessories.",
      "product_quantity": "313,190 (total for all devices)",
      "reason_for_recall": "ConMed received complaints of some devices which had broken through the seal of the sterile pouch.  ConMed confirmed instances where the pouch seal was compromised on the affected products.  In no instance has it been reported to ConMed that a compromise in the sterile barrier has resulted in illness or injury.  The compromised seals were discovered prior to use.",
      "recall_initiation_date": "20121227",
      "center_classification_date": "20130124",
      "termination_date": "20180514",
      "report_date": "20130130",
      "code_info": "Beginning Lot Code 120628X, Ending Lot Code 120917X. [Lot codes on boxes and packaging contain a lot code in the following format: 120917X  where 12 represents the year (2012), 09 represents the month (September), 17 represents the day of the month, and X represents the manufacturing shift code (1, 2, 3, 4,5,6 or 9)]."
    }
  ]
}