{
  "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": "Wayne",
      "address_1": "45 Barbour Pond Dr",
      "reason_for_recall": "In the Cardiosave Intra-aortic Balloon Pump, there is a possibility that the coiled cord assembly, a prominent connector cord between the Cardiosave IABP housing and the dual display head which secured atop the IABP may fail as a result of mishandling.",
      "address_2": "",
      "product_quantity": "29 units (total)",
      "code_info": "510K K112372  Device Listing Number  D132687      US Customer IABPs  CA202159K1  CA202167K1  CA203492L1  CA203494L1    International Customer IABPs  CA203486L1  CA202155K1  CA202161K1  CA203487L1  CA203490L1  CA203507L1  CA204330L1  CA204328L1  CA203505L1    International Company Owned IABPs    CA204327L1  CA202150K1  CA203506L1  CA204324L1  CA204326L1  CA202163K1  CA202169K!  CA203497L1  CA203498L1  CA203496L1  CA203503L1  CA203488L1  CA203493L1  CA203508L1  CA204337L1  CA203502L1",
      "center_classification_date": "20130109",
      "distribution_pattern": "Worldwide Distribution - USA including ID and Fl and Internationally to United Arab Emirates, France, Luxembourg, Poland, Spain, Sweden, Germany, Italy, Netherlands, Republic of China, Spain, Sweden, and Thailand",
      "state": "NJ",
      "product_description": "CARDIOSAVE Intra-Aortic Balloon Pump    An electromechanical system used to inflate and deflate intra-aortic balloons. It provide temporary support to the left ventricle via the principle of counterpulsation.",
      "report_date": "20130116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Maquet Cardiovascular, LLC",
      "recall_number": "Z-0662-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62121",
      "termination_date": "20150930",
      "more_code_info": "",
      "recall_initiation_date": "20120327",
      "postal_code": "07470-2094",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}