{
  "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": "Austin",
      "address_1": "7000 W William Cannon Dr",
      "reason_for_recall": "A sharp edge on the cannulated tip of the device may damage or cut a suture.",
      "address_2": "",
      "product_quantity": "76",
      "code_info": "Catalog #25-3011, Lot #1049402",
      "center_classification_date": "20140109",
      "distribution_pattern": "Worldwide distribution: US (nationwide) including states of: CA, FL, GA, IL, IN, KY, MN, MO, NY, OH, TX, and WI. Internationally to: Canada, France, Germany, Spain, and Switzerland.",
      "state": "TX",
      "product_description": "Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only",
      "report_date": "20140115",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ArthroCare Medical Corporation",
      "recall_number": "Z-0652-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67087",
      "termination_date": "20150408",
      "more_code_info": "",
      "recall_initiation_date": "20131209",
      "postal_code": "78735-8509",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}