{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Goteborg",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90143",
      "recalling_firm": "XVIVO PERFUSION AB",
      "address_1": "Massans Gata 10",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: CA, FL, MA, NC, NY, OH, PA, and TX     O.U.S.: Austria, Canada, France, Ireland, Italy, and the Netherland",
      "recall_number": "Z-1212-2022",
      "product_description": "XVIVO Organ Chamber REF 19020",
      "product_quantity": "80 devices",
      "reason_for_recall": "The weld seal of the primary pouch was incomplete, and the sterility of the product cannot be ensured/guaranteed.",
      "recall_initiation_date": "20220408",
      "center_classification_date": "20220601",
      "termination_date": "20250130",
      "report_date": "20220608",
      "code_info": "Model Number: 19020  Lot Numbers/UDI Codes:  LOT: 13801, UDI: (01)07350069520074(17)240930(10)13801  LOT: 13802, UDI: (01)07350069520074(17)240930(10)13802  LOT: 13803, UDI: (01)07350069520074(17)240930(10)13803  LOT: 13804, UDI: (01)07350069520074(17)240930(10)13804  LOT: 13805, UDI: (01)07350069520074(17)240930(10)13805  LOT: 13806, UDI: (01)07350069520074(17)240930(10)13806"
    }
  ]
}