{
  "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": "Mansfield",
      "address_1": "15 Hampshire Street",
      "reason_for_recall": "On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion.  CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in specific convenience kits.",
      "address_2": "",
      "product_quantity": "17740 kits",
      "code_info": "Product 80530: 032887164, 203184264,110983764, 208286764, 116480564, 221590564, 120987864, 236385564,127085464; Product 8508: 207383964, 23489464",
      "center_classification_date": "20130511",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) and in the country of: Panama.",
      "state": "MA",
      "product_description": "Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508.    IV Start Kit.",
      "report_date": "20130522",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Covidien LLC",
      "recall_number": "Z-1303-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64908",
      "termination_date": "20150602",
      "more_code_info": "",
      "recall_initiation_date": "20130412",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}