{
  "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": "2026-04-08",
    "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": "83927",
      "recalling_firm": "Datascope Corp.",
      "address_1": "1300 Macarthur Blvd",
      "address_2": "N/A",
      "postal_code": "07430-2052",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to CA, GA, and TX.",
      "recall_number": "Z-0266-2020",
      "product_description": "Low Level Output Cable   Interface to Philips Monitor For Use With Cardiosave and CS300 Intra-Aortic Balloon  Pumps (IABPs), Part Number 0012-00-1589-03",
      "product_quantity": "7",
      "reason_for_recall": "One lot of \"Low Level Output Cable - Interface to Philips Monitor\" was received from the supplier with an incorrect cable in the packaging.",
      "recall_initiation_date": "20191003",
      "center_classification_date": "20191101",
      "termination_date": "20210108",
      "report_date": "20191113",
      "code_info": "10000493876"
    }
  ]
}