{
  "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": "Fairfield",
      "address_1": "15 Law Dr",
      "reason_for_recall": "55 kits were distributed after their expiration date of September 2015.",
      "address_2": "",
      "product_quantity": "55 units",
      "code_info": "Lot/batch number: 3000001571  UDI code: 607567206489",
      "center_classification_date": "20180130",
      "distribution_pattern": "Distributed to the states of NM, CA, and IL.",
      "state": "NJ",
      "product_description": "Hemofiltration Standard Pack including BC 60 Plus-T 8036.  Part Number: 701066990.    Used in extracorporeal circulation during cardiopulmonary bypass procedures lasting 6 hours or less.",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Maquet",
      "recall_number": "Z-0490-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78765",
      "termination_date": "20180712",
      "more_code_info": "",
      "recall_initiation_date": "20170522",
      "postal_code": "07004-3206",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}