{
  "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": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86503",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including in the states of CA, CO, CT, OH, TX, and NY.",
      "recall_number": "Z-0068-2021",
      "product_description": "Kit Model #65193091, MTO Left Heart Kit - Product Usage: NAMIC Cath Lab and Interventional Radiology (IR) Kits consist of any combination of devices from the NAMIC Fluid Management finished good product families and potentially other devices designed and manufactured by original equipment manufacturers (OEM).",
      "product_quantity": "16 kits",
      "reason_for_recall": "Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.",
      "recall_initiation_date": "20200914",
      "center_classification_date": "20201007",
      "termination_date": "20210409",
      "report_date": "20201014",
      "code_info": "Lot 5619215, Exp 06/30/2023"
    }
  ]
}