{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Research Triangle Park",
      "address_1": "2917 Weck Dr",
      "reason_for_recall": "Some boxes are labeled as containing Visistat Wide devices, when they in fact they contained Visistat Regular device.",
      "address_2": "",
      "product_quantity": "3594 eaches",
      "code_info": "73H1600207",
      "center_classification_date": "20170517",
      "distribution_pattern": "Worldwide Distribution - US including CA, FL, GA, IL, IN, KS, KY, ME, MD, MA, MI, NJ, NY, NC, OH, OR, RI, TX, UT, VA, and Internationally to Australia, Belgium and France",
      "state": "NC",
      "product_description": "WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO,    Visistat is indicated for the external skin closure of lacerations on the outer layer of the dermis for a wide range of general, thoracic, obstetric, gynecological, orthopedic, cardiovascular, urological, and plastic surgical procedures",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teleflex Medical",
      "recall_number": "Z-2108-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77102",
      "more_code_info": "",
      "recall_initiation_date": "20170324",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Completed"
    }
  ]
}