{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72860",
      "recalling_firm": "Arkray Factory USA, Inc.",
      "address_1": "5182 W 76th St",
      "address_2": "N/A",
      "postal_code": "55439-2900",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of FL, IL, KY, MI, NC, NY, OH, and TN.",
      "recall_number": "Z-0630-2016",
      "product_description": "arkray SPOTCHEM II Glucose Reagent test strips, Item No. 77101, MEDTEST DX Catalog # 77424.      For the in vitro quantitative determination of glucose in human plasma from whole blood samples.",
      "product_quantity": "88 boxes (25 foil packaged test strips per box)",
      "reason_for_recall": "One lot each of SPOTCHEM II Basic PANEL-1 Reagent Test Strip and SPOTCHEM II Glucose Reagent Test Strip are being recalled due to a lowered reaction rate in the reagent pad for glucose.  The affected lots will display a result of approximately 300 to 400 mg/dL for any glucose value that exceeds the upper limit of 416 mg/dL.",
      "recall_initiation_date": "20151218",
      "center_classification_date": "20160115",
      "termination_date": "20170104",
      "report_date": "20160127",
      "code_info": "Lot Number EA4M78",
      "more_code_info": ""
    }
  ]
}