{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Elkton",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68024",
      "recalling_firm": "Terumo Cardiovascular Systems Corporation",
      "address_1": "125 Blue Ball Rd",
      "address_2": "N/A",
      "postal_code": "21921-5315",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-2029-2014",
      "product_description": "Sarns Disposable Centrifugal Pump with X-Coating, 164275X, is a sterile, single use device.    For use in cardiopulmonary bypass procedures.",
      "product_quantity": "N/A",
      "reason_for_recall": "During set-up and priming of the bypass circuit, leaks were detected on the centrifugal pumphead.",
      "recall_initiation_date": "20140414",
      "center_classification_date": "20140711",
      "termination_date": "20160907",
      "report_date": "20140723",
      "code_info": "Lot No. RC07, QM03, QN07, and RA09."
    }
  ]
}