{
  "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": "Itasca",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84880",
      "recalling_firm": "Organ Recovery Systems, Inc.",
      "address_1": "1 Pierce Pl Ste 475W",
      "address_2": "N/A",
      "postal_code": "60143-2618",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed nationwide (32 states) and to Canada.",
      "recall_number": "Z-1437-2020",
      "product_description": "LKT200 Perfusion Circuit, part of Lifeport Kidney Perfusion Transporter KTR - Product Usage: The circuit is an accessory to LifePort Kidney Perfusion Transporter (KTR) Isolated kidney perfusion and transport system, which is intended to be used for the continuous hypothermic machine perfusion of kidneys for the preservation, transportation and eventual transplantation into a recipient.",
      "product_quantity": "2274",
      "reason_for_recall": "Observed leakage at the sample port assembly which could potentially lead to loss of perfusion solution needed to maintain continuous machine perfusion.",
      "recall_initiation_date": "20200130",
      "center_classification_date": "20200304",
      "termination_date": "20210930",
      "report_date": "20200311",
      "code_info": "LKT2000 Lots 119944, 119765, 119648, 120055, 120242."
    }
  ]
}