{
  "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": "Ongoing",
      "city": "Dublin",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87787",
      "recalling_firm": "Cardinal Health Inc.",
      "address_1": "7000 Cardinal Pl",
      "address_2": "N/A",
      "postal_code": "43017-1091",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of FL, GA, SC.",
      "recall_number": "Z-1936-2021",
      "product_description": "ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT  Item Number: 2990174",
      "product_quantity": "5,356 boxes of 100 strips",
      "reason_for_recall": "Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.",
      "recall_initiation_date": "20210316",
      "center_classification_date": "20210623",
      "report_date": "20210630",
      "code_info": "NDC/UPC: 353885009713  All lots numbers shipped from 2/23/201 to 3/10/2021"
    }
  ]
}