{
  "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": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70510",
      "recalling_firm": "Maquet Datascope Corp - Cardiac Assist Division",
      "address_1": "1300 MacArthur Blvd.",
      "address_2": "N/A",
      "postal_code": "07430-2052",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution",
      "recall_number": "Z-1140-2015",
      "product_description": "Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP)",
      "product_quantity": "1,300 units",
      "reason_for_recall": "Power supply malfunction complaints related to suboptimal thermal management.",
      "recall_initiation_date": "20150130",
      "center_classification_date": "20150223",
      "termination_date": "20170929",
      "report_date": "20150304",
      "code_info": "0998-00-0800-31 0998-UC-0800-31  0998-00-0800-32 0998-UC-0800-33  0998-00-0800-33 0998-UC-0800-52  0998-00-0800-34 0998-UC-0800-53  0998-00-0800-35 0998-UC-0800-55  0998-00-0800-45  0998-00-0800-52  0998-00-0800-53  0998-00-0800-55.      CARDIOSAVE Hybrid IABPs serviced with a new/replacement power supply after August 19, 2014 are not affected.",
      "more_code_info": ""
    }
  ]
}