{
  "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 I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82124",
      "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": "US nationwide and Canada. US distribution to the following states:  AZ, FL, IL, IN, KS, MA, MI, MO, PA, SC, TN, and WA.    The products were distributed to the following foreign countries:  Canada.",
      "recall_number": "Z-0979-2019",
      "product_description": "Cook Transseptal Needle, Reference Number TSNC-18-71.0, Order Number G02364.  For transseptal left heart access in both diagnostic and interventional procedures.",
      "product_quantity": "100",
      "reason_for_recall": "The products were manufactured without a back bevel on the needle tip. This could cause damage to the inside of the introducer during needle insertion.",
      "recall_initiation_date": "20190201",
      "center_classification_date": "20190313",
      "termination_date": "20200630",
      "report_date": "20190320",
      "code_info": "Lot 8833687"
    }
  ]
}