{
  "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": [
    {
      "country": "United States",
      "city": "Bloomington",
      "address_1": "750 N Daniels Way",
      "reason_for_recall": "Affected products may have been manufactured with the catheter distal end hole too small",
      "address_2": "",
      "product_quantity": "83 kits",
      "code_info": "Lot Numbers  7716007  7703324  NS7703501  NS7703502  NS7703503  NS7704718  NS7704722  NS7704727  NS7704728",
      "center_classification_date": "20190604",
      "distribution_pattern": "Domestically: OH;     Internationally: CANADA, SPAIN, ITALY, BELGIUM, GERMANY, UNITED ARAB EMIRATES, GREECE, SWITZERLAND, OMAN, MONACO, SAUDI ARABIA,  AUSTRALIA, HONG KONG, INDIA & KOREA",
      "state": "IN",
      "product_description": "Pericardiocentesis Catheter Set, RPN C-PCS-850, Order # G03282",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cook Inc.",
      "recall_number": "Z-1722-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82692",
      "termination_date": "20200428",
      "more_code_info": "",
      "recall_initiation_date": "20190409",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}