{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Brooklyn Park",
      "address_1": "7611 Northland Dr N",
      "reason_for_recall": "Affected products failed a sterilization test.",
      "address_2": "",
      "product_quantity": "10 units",
      "code_info": "Lot# 215729283",
      "center_classification_date": "20200704",
      "distribution_pattern": "Domestic Distribution only to CA and MI.",
      "state": "MN",
      "product_description": "Extra corporeal circuit with bio-active surface.",
      "report_date": "20200715",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Perfusion Systems",
      "recall_number": "Z-2495-2020",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "85821",
      "termination_date": "20201006",
      "more_code_info": "",
      "recall_initiation_date": "20180808",
      "postal_code": "55428-1088",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}