{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bloomington",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90710",
      "recalling_firm": "Cook Incorporated",
      "address_1": "750 N Daniels Way",
      "address_2": "",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Foreign: AR AT AU BE  BG CA CA  CH CL CN CZ  DE  DK ES  FR  GB GR  GU HU  IL IT  JO  JP KR KW MX MY NC NL PE PL PR PT  PY RU  SE SI TR UY ZA",
      "recall_number": "Z-1717-2022",
      "product_description": "Roadrunner UniGlide Hydrophilic Wire Guide    REFERENCE PART NUMBER (RPN): HPWS-35-150    ORDER NUMBER (GPN): G56152.   For vascular catheter positioning and exchange in diagnostic and interventional procedures.",
      "product_quantity": "30 units",
      "reason_for_recall": "Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.",
      "recall_initiation_date": "20220719",
      "center_classification_date": "20220909",
      "report_date": "20220921",
      "code_info": "UDI-DI: (01)00827002561526-  Lot Numbers: 14118842",
      "more_code_info": ""
    }
  ]
}