{
  "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": "Fairfield",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80086",
      "recalling_firm": "Datascope Corporation",
      "address_1": "15 Law Dr",
      "address_2": "N/A",
      "postal_code": "07004-3206",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states: AL, OR, and TX.",
      "recall_number": "Z-2104-2018",
      "product_description": "Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET, Part Number 701054588",
      "product_quantity": "19 total kits",
      "reason_for_recall": "There is a potential problem with the cuvette where failure of the cuvette would cause an error message on the  monitor display of H/S DISCONNECT AT CUVETTE.",
      "recall_initiation_date": "20160311",
      "center_classification_date": "20180606",
      "termination_date": "20190607",
      "report_date": "20180613",
      "code_info": "Batch Number 3000020069, UDI Code 10607567203300;    Batch Number 3000021675, UDI Code 10607567203300"
    }
  ]
}