{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Charlotte",
      "address_1": "301 Mccullough Dr",
      "reason_for_recall": "Failure to submit a 510(k) for device labeling changes.",
      "address_2": "Suite 400",
      "product_quantity": "7175 units",
      "code_info": "U14030713, 814031313, U140312323, and U14031413.",
      "center_classification_date": "20141223",
      "distribution_pattern": "US Distribution to the states of FL and OH.",
      "state": "NC",
      "product_description": "UniStrip1, Blood Glucose Test Strips, 50 count box.    The test strips are indicated for use by people with diabetes in their home as an aid to monitor the effectiveness of diabetes control.",
      "report_date": "20141231",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Unistrip Technologies LLC",
      "recall_number": "Z-0855-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69856",
      "termination_date": "20150520",
      "more_code_info": "",
      "recall_initiation_date": "20141120",
      "postal_code": "28262-3310",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}