{
  "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-0216-2016",
      "product_description": "ELITech Clinical Systems reagents used on the Selectra ProS and ProM systems that utilize the Trinder Reaction method.    The following product reference numbers and names:    GPSL-025O:  Glucose PAP SL  AUML-0250: URIC ACID MONO SL  CHSL-0250: CHOLESTEROL SL,  TGML-0250: TRIGLYCERIDES SL,  CRSL-0250: CREATININE PAP SL  HDLL-0230: CHOLESTEROL HDL SL 2G  LDLL-0230: CHOLESTEROL LDL SL 2G",
      "product_quantity": "969 systems",
      "reason_for_recall": "ELITech Clinical Systems reagents based on Trinder reaction used on the Selectra ProS and ProM systems 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"
    }
  ]
}