{
  "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": "2026-07-08",
    "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": "94274",
      "recalling_firm": "Medtronic Perfusion Systems",
      "address_1": "7611 Northland Dr N",
      "address_2": "N/A",
      "postal_code": "55428-1088",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.",
      "recall_number": "Z-1796-2024",
      "product_description": "Medtronic I.M.A. Cannulae:  DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001",
      "product_quantity": "7935 units",
      "reason_for_recall": "Potential for unsealed sterile packing.",
      "recall_initiation_date": "20240319",
      "center_classification_date": "20240510",
      "report_date": "20240522",
      "code_info": "GTIN 00613994575319, Lot Numbers:  2023041320, 2023041323; GTIN 00673978180465, Lot Numbers:  2023041316, 2023041323; GTIN 20613994575313, Lot Numbers:   2023041316, 2023041318, 2023041320, 2023041323, 202305C146, 202305C154"
    }
  ]
}