{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82737",
      "recalling_firm": "Arkray Factory USA, Inc.",
      "address_1": "5182 W 76th St",
      "address_2": "N/A",
      "postal_code": "55439-2900",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US",
      "recall_number": "Z-1850-2019",
      "product_description": "AUTION HYBRID AU-4050",
      "product_quantity": "159 units",
      "reason_for_recall": "This correction is being initiated due to a software issue which results in the possibility of incorrect patient information being assigned to sample results when the following rare combination of three specific events were to occur:   1) No measurement results are generated due to an error by a urine sediment measurement.  2) The instrument is shutdown incorrectly.  3) An item rack is used for subsequent sample measurements.",
      "recall_initiation_date": "20190503",
      "center_classification_date": "20190620",
      "termination_date": "20200917",
      "report_date": "20190626",
      "code_info": "UDI:  (01) 00015482146030  All serial numbers"
    }
  ]
}