{
  "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": "Hazelwood",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84464",
      "recalling_firm": "Biomerieux Inc",
      "address_1": "595 Anglum Rd",
      "address_2": "N/A",
      "postal_code": "63042-2320",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US",
      "recall_number": "Z-0928-2020",
      "product_description": "BIOMERIEUX VIDAS 3, Compact immunoanalyzer with full traceability and automation",
      "product_quantity": "738 units",
      "reason_for_recall": "Following Customers complaints, investigations have been initiated on potentially false results obtained on VIDAS 3 with an expired calibration.   Indeed, the calibrations of assays were valid in the calibration menu whereas in fact the calibrations were expired  and no alarm displayed to warn the users about the expiration date of the calibrations. Software computes results of analysis for assays with expired calibrations.   The  anomaly is due to an incorrect update of the calibration status by the software.",
      "recall_initiation_date": "20191022",
      "center_classification_date": "20200131",
      "termination_date": "20240806",
      "report_date": "20200212",
      "code_info": "software versions 1.2 and higher"
    }
  ]
}