{
  "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": [
    {
      "country": "United States",
      "city": "Fairfield",
      "address_1": "15 Law Dr",
      "reason_for_recall": "During label reconciliation a duplicate serial number label was detected to be printed for the LINEAR 7.5 FR 40 cc Intra-Aortic Balloon Catheter.",
      "address_2": "",
      "product_quantity": "one unit",
      "code_info": "Part Number - 0684-00-0480-01U",
      "center_classification_date": "20140903",
      "distribution_pattern": "US Distribution to TX.",
      "state": "NJ",
      "product_description": "LINEAR 7.5 FR. 40cc IAB Catheter   Maquet Getinge Group",
      "report_date": "20140910",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Datascope Corporation",
      "recall_number": "Z-2568-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69072",
      "termination_date": "20150205",
      "more_code_info": "",
      "recall_initiation_date": "20140811",
      "postal_code": "07004-0011",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}