{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ft Lauderdale",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85535",
      "recalling_firm": "Trividia Health, Inc.",
      "address_1": "2400 NW 55th Ct",
      "address_2": "N/A",
      "postal_code": "33309-2672",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "US Nationwide distribution including in the state of Florida.",
      "recall_number": "Z-2201-2020",
      "product_description": "TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: is intended for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip or forearm.",
      "product_quantity": "1 unit",
      "reason_for_recall": "One (1) TRUE METRIX AIR blood glucose meter distributed in the United States was packaged into a TRUE METRIX blood glucose meter kit and has an incorrect factory-set unit of measure;  the meter displays glucose results in mmol/L rather than mg/dL.",
      "recall_initiation_date": "20200420",
      "center_classification_date": "20200601",
      "termination_date": "20210601",
      "report_date": "20200610",
      "code_info": "Serial Number TA1548753"
    }
  ]
}