{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Brooklyn Park",
      "address_1": "7611 Northland Dr N",
      "reason_for_recall": "Medtronic has identified an out of-specification condition exhibiting excess plastic (flash) in the arterial filter directly above the outlet port.",
      "address_2": "",
      "product_quantity": "24 units",
      "code_info": "UDI 20643169858835, Lot Numbers:  13316512",
      "center_classification_date": "20191217",
      "distribution_pattern": "CA",
      "state": "MN",
      "product_description": "Medtronic Affinity, 38um Arterial Filter, Catalog number REF 351",
      "report_date": "20191225",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Perfusion Systems",
      "recall_number": "Z-0693-2020",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "84410",
      "termination_date": "20201005",
      "more_code_info": "",
      "recall_initiation_date": "20191114",
      "postal_code": "55428-1088",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}