{
  "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": [
    {
      "country": "United States",
      "city": "Durham",
      "address_1": "100 Rodolphe St",
      "reason_for_recall": "Complaints were received from customers observing falsely overestimate results or external quality control higher results than expected when performing tests with VIDAS Testosterone.",
      "address_2": "",
      "product_quantity": "742",
      "code_info": "Lots 1004878310 & 1005001080",
      "center_classification_date": "20170711",
      "distribution_pattern": "AR, CA, CO, GA, IL, IA, MI, MN, MT, NY, OK, TN, TX, WY, Columbia, Costa Rica, El Salvador, France, Hong Kong, Jordan, Nicaragua, Russian Fed., Sri Lanka, Sweden, Ukraine",
      "state": "NC",
      "product_description": "VIDAS Testosterone, Ref 30418",
      "report_date": "20170719",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "bioMerieux, Inc.",
      "recall_number": "Z-2339-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77292",
      "termination_date": "20200611",
      "more_code_info": "",
      "recall_initiation_date": "20170515",
      "postal_code": "27712-9402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}