{
  "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": "Oyster Bay",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74614",
      "recalling_firm": "Circulatory Technology Inc",
      "address_1": "21 Singworth St",
      "address_2": "N/A",
      "postal_code": "11771-3703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution to states of: AL, AR, CA, Washington, D.C., FL, GA, IA, IL, IN, KY, LA, MI, MS, NC, NJ, NY, OH, OK, PA, SC, TN, TX & VA.",
      "recall_number": "Z-0057-2017",
      "product_description": "The Better-Bladder With 14\" ID tubing, ITEM BB14, STERILE,    Measure pressure noninvasively in the extracorporeal circuit and provide compliance in the venous line between the patient and the pump.",
      "product_quantity": "958 units",
      "reason_for_recall": "Twisted or wrinkled balloon components which are considered a cosmetic defect by the firm.",
      "recall_initiation_date": "20160701",
      "center_classification_date": "20161007",
      "termination_date": "20170414",
      "report_date": "20161019",
      "code_info": "Lot Numbers: R19229, 015323, 014882, 014602 & 014601"
    }
  ]
}