{
  "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": "SEES",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72322",
      "recalling_firm": "ELITech Clinical Systems SAS",
      "address_1": "Zone lndustrielle",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0215-2016",
      "product_description": "Eon 300 system includes the following product reference numbers and names:    Reference no. 79345\tGlucose (GPSL)  Reference no. 79450\tUric acid (AUVD)  Reference no. 79435\tTriglycerides (TGML)   Reference no. 79295\tCholesterol (CHVD)  Reference no. 79301\tCholesterol HDL (HDLL)   Reference no. 79310\tCholesterol, LDL (LDLL)",
      "product_quantity": "612 total",
      "reason_for_recall": "ELITech clinical Systems reagents based on Trinder reaction used on the Eon 300 instrument system are recalled due to potential drug interference.  No complaints were received.",
      "recall_initiation_date": "20150922",
      "center_classification_date": "20151104",
      "termination_date": "20160304",
      "report_date": "20151111",
      "code_info": "all lots"
    }
  ]
}