{
  "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": "Research Triangle Park",
      "address_1": "2917 Weck Dr",
      "reason_for_recall": "Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices.  The 6 individually packaged units within the boxes are correctly labeled.",
      "address_2": "",
      "product_quantity": "12 units",
      "code_info": "Lot Number 73H1600207",
      "center_classification_date": "20180326",
      "distribution_pattern": "KS",
      "state": "NC",
      "product_description": "Teleflex MEDICAL WECK Visistat 35.  Used for the external skin closure of lacerations.",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teleflex Medical",
      "recall_number": "Z-1193-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79301",
      "termination_date": "20181031",
      "more_code_info": "",
      "recall_initiation_date": "20180215",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}