{
  "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": "2026-04-15",
    "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": "82910",
      "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": "No distribution in the US.    Products were distributed to the following foreign countries: China.",
      "recall_number": "Z-1780-2019",
      "product_description": "Neff Percutaneous Access Set, Catalog Number NPAS-100-RH-NT",
      "product_quantity": "97",
      "reason_for_recall": "The products may have been manufactured without the bottom seal on the outer packaging, compromising the sterility of the product.",
      "recall_initiation_date": "20190502",
      "center_classification_date": "20190613",
      "termination_date": "20190823",
      "report_date": "20190619",
      "code_info": "lot 8373482"
    }
  ]
}