{
  "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-0217-2016",
      "product_description": "Envoy 500 system includes the following product reference numbers and names:     55345\tENVOY 500 Glucose  55450\tENVOY 500 URIC ACID REAGENT KIT  55435\tENVOY 500 TRIGLYCERIDES REAGENT KIT,  55297\tENVOY 500 CHOLESTEROL REAGENT KIT,  55335\tENVOY 500 CREATININE REAGENT KIT  55301\tENVOY 500 HDL CHOLESTEROL REAGENT  55310\tENVOY 500 LDL CHOLESTEROL REAGENT KIT",
      "product_quantity": "13455 systems",
      "reason_for_recall": "ELITech clinical Systems reagents based on Trinder reaction used on the Envoy 500 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"
    }
  ]
}