{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "48805",
      "product_res_number": "Z-0096-2007",
      "event_date_initiated": "2006-10-12",
      "event_date_posted": "2006-10-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-08-30",
      "res_event_number": "36515",
      "product_code": "GEJ",
      "k_numbers": [
        "K943327"
      ],
      "product_description": "ConMed Laparoscopic Instrument: Babcock Disposable Grasper, 5mm x 43cm length, REF/Product Code 60-6047-431. --- The product is distributed sterile in heat-sealed tray and labeled with an expiration date that pertains only to the sterility.",
      "code_info": "REF/Product Code 60-6047-431, all lot codes manufactured between 08/25/2003 and 03/24/2005. [Lot codes on unopened boxes and packaging contain a lot code in the following form: for example 0409271 - 04 represents the year 2004, 09 represents the month of the year, 27 represents the day of the month, and the last digit 1 represents the manufacturing shift code. Lot codes are located on the device in this form: for example 40927 - 4 represents the year 2004, 09 represents the month of the year, and 27 represents the day of the month.]",
      "firm_fei_number": "3001451571",
      "recalling_firm": "Conmed Corporation",
      "address_1": "525 French Road",
      "city": "Utica",
      "state": "NY",
      "postal_code": "13502-5945",
      "additional_info_contact": "Ms. Patricia Cotter\n315-624-3533",
      "reason_for_recall": "The grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "On 10/12/06, ConMed sent \"URGENT DEVICE RECALL\" packages (letter dated 10/11/06) to the domestic accounts via UPS Ground, and via UPS Express for the International accounts. Devices are to be removed from use and returned.",
      "product_quantity": "32 units",
      "distribution_pattern": "Worldwide",
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        "device_name": "Carrier, Ligature",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4800",
        "device_class": "1"
      }
    }
  ]
}