{
  "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": "Ongoing",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86575",
      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "15 Hampshire St Bldg 5",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0452-2021",
      "product_description": "Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutritional feeding product.",
      "product_quantity": "314460",
      "reason_for_recall": "The feeding spike sets may leak at the interface of the tube and spike connector.",
      "recall_initiation_date": "20200922",
      "center_classification_date": "20201113",
      "report_date": "20201125",
      "code_info": "All lots of products manufactured in the below timespan:  July 1, 2015 and July 20, 2019"
    }
  ]
}