{
  "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": "Roskilde",
      "state": "",
      "country": "Denmark",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74242",
      "recalling_firm": "Unomedical As",
      "address_1": "Aholmvej 1  3 Osted",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US including CA, IN, PA, and Internationally  to Canada, Korea, and Japan.",
      "recall_number": "Z-0358-2017",
      "product_description": "Comfort 5+5 Pack w/110cm Tube & 17mm Cann. UPC# 3-89110-14147-7; Comfort 5+5 Pack w/60cm Tube & 17mm Cann. UPC# 3-89110-14127-9; Comfort 5+5 Pack w/110cm Tube & 13mm Cann. UPC# 3-89110-14143-9; Conform 5+5 Pack w/60cm Tube & 13mm Cann. UPC# 3-89110-14123-1  The products are used in combination with insulin infusion pumps for continuous subcutaneous infusion of insulin",
      "product_quantity": "22,114 units",
      "reason_for_recall": "Tubing detachment",
      "recall_initiation_date": "20141107",
      "center_classification_date": "20161103",
      "termination_date": "20161116",
      "report_date": "20161109",
      "code_info": "5048997, 5048998, 5048999, 5052118, 5052332, 5052333, 5052334, 5063721, 5066962, 5066963, 5066964",
      "more_code_info": ""
    }
  ]
}