{
  "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": [
    {
      "status": "Terminated",
      "city": "Arvada",
      "state": "CO",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79000",
      "recalling_firm": "LivaNova USA",
      "address_1": "14401 W 65th Way",
      "address_2": "N/A",
      "postal_code": "80004-3503",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to one consignee in LA.",
      "recall_number": "Z-0664-2018",
      "product_description": "Sorin Group Smart Perfusion Pack E-Pack, REF 088511400, Rev: L, Single Use, Sterile, Rx.  The firm name on the label is Sorin Group USA, Inc., Arvada, CO.",
      "product_quantity": "16 units (6 from lot 1717800062 and 10 units from lot 1720800071",
      "reason_for_recall": "The product is labeled with the incorrect expiration date.",
      "recall_initiation_date": "20171219",
      "center_classification_date": "20180221",
      "termination_date": "20200811",
      "report_date": "20180228",
      "code_info": "Lot 1717800062, UDI (01)00803622108075(240)088511400(17)190630(10)1717800082; and Lot 1720800071, UDI (01)00803622108075(240)088511400(17)190731(10)1720800071"
    }
  ]
}