{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Brooklyn Park",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99199",
      "recalling_firm": "Medtronic Perfusion Systems",
      "address_1": "7611 Northland Dr N",
      "address_2": "",
      "postal_code": "55428-1088",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.",
      "recall_number": "Z-2738-2026",
      "product_description": "Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula",
      "product_quantity": "",
      "reason_for_recall": "Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.",
      "recall_initiation_date": "20260525",
      "center_classification_date": "20260715",
      "report_date": "20260722",
      "code_info": "MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220",
      "more_code_info": ""
    }
  ]
}