{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bloomington",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82795",
      "recalling_firm": "Cook Inc.",
      "address_1": "750 N Daniels Way",
      "address_2": "N/A",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign:  Australia  Canada  Austria  Belgium  Denmark  Germany  Spain  Finland  France  Martinique  French Polynesia  Switzerland  Ireland  Italy  Netherlands  Poland  Sweden  United Kingdom  Hong Kong  New Zealand  Chile  Colombia  Israel  Russian Federation  Czech Republic  Greece  Jordan  Slovakia  South Africa  United Arab Emirates  Slovenia  Lithuania  Morocco  Romania  Qatar  Bulgaria  Libya  Saudi Arabia  Turkey  Ukraine  Thailand",
      "recall_number": "Z-1369-2019",
      "product_description": "Cook Kwart Retro-Inject Ureteral Stent Set:  PRODUCT/CATALOG NUMBER/GPN:   4.7 Fr   003500  G14916;  6.0 Fr   003600  G14836;  7.0 Fr   003700  G14837;  8.0 Fr   003800  G14844;    Set with AQ¿ Hydrophilic Coating  PRODUCT/CATALOG NUMBER/GPN:  4.7 Fr    AQ-003500  G17150;  6.0 Fr    AQ-003600 G17151;  7.0 Fr    AQ-003700 G17152",
      "product_quantity": "12968",
      "reason_for_recall": "Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative Pyeloplasty Stent Set  Instructions for Use (IFU) did not include a warning for stent knotting.",
      "recall_initiation_date": "20190422",
      "center_classification_date": "20190517",
      "termination_date": "20200505",
      "report_date": "20190529",
      "code_info": "All lot codes"
    }
  ]
}