{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82265",
      "recalling_firm": "Maquet Cardiovascular Us Sales, Llc",
      "address_1": "45 Barbour Pond Dr",
      "address_2": "N/A",
      "postal_code": "07470-2094",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US Nationwide Distribution in the states of California, Florida, Illinois, Kentucky, Michigan, and New York.",
      "recall_number": "Z-0986-2019",
      "product_description": "Cardiohelp Emergency Drive, Part No. 70104.8002    Product Usage:  The Cardiohelp Emergency Drive is used in emergencies to manually drive the disposable if the Cardiohelp-i fails.",
      "product_quantity": "10",
      "reason_for_recall": "Upon servicing the gearwheel in the Emergency Drive the gearwheel may have been re-assembled  incorrectly, leading to the inadequate operation of the Emergency Drive.",
      "recall_initiation_date": "20190208",
      "center_classification_date": "20190328",
      "termination_date": "20200514",
      "report_date": "20190403",
      "code_info": "Affected serial numbers:  90420359, 90421204, 90421188, 90421279, 90421228, 90421761, 90420904, 90420231,  90420455, 90421304"
    }
  ]
}