{
  "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": "72890",
      "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": "Worldwide Distribution- Nationwide Distribution including Puerto Rico.",
      "recall_number": "Z-1248-2016",
      "product_description": "Cardiosave Hybrid and rescue IABP",
      "product_quantity": "1243 units US; 1107 units OUS",
      "reason_for_recall": "Maquet has recieved information that in some Cardiosave IABPS, the scroll compressor did not meet the specifications for output pressure or vacuum at specific flow rates.",
      "recall_initiation_date": "20151216",
      "center_classification_date": "20160325",
      "termination_date": "20180601",
      "report_date": "20160406",
      "code_info": "Cardiosave Hybrid IABP 0998-00-0800-53,0998-UC-0800-53, Cardiosave Rescue IABP 0998-00-0800-83 & 0998-UC-0800-83"
    }
  ]
}