{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96091",
      "recalling_firm": "Dexcom, Inc.",
      "address_1": "6340 Sequence Dr",
      "address_2": "N/A",
      "postal_code": "92121-4356",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of OH, TX, PA, MN, SC, NH, FL, CA, NJ, PR, GA and the countries of Austria, Belgium, Canada, Switzerland, Germany, Spain, France, Ireland, Japan, Netherlands, Slovenia, United Kingdom,  Australia, Czech Republic, Denmark, Finland, France, Hong Kong, Israel, Italy, Korea, Kuwait, New Zealand, Norway, Oman, Poland, Qatar, Saudi Arabia, Singapore, Slovakia, South Africa, Sweden, Turkey, United Arab Emirates.",
      "recall_number": "Z-1202-2025",
      "product_description": "Dexcom G6, Continuous Glucose Monitoring System, REFs: STK-OM-001, STR-OM-001, STR-OR-001",
      "product_quantity": "N/A",
      "reason_for_recall": "Under very rare situations, the Dexcom G6 touchscreen receiver may not provide high or low glucose  alarms/alerts as designed, which can result in two different conditions. First, if a receiver operating system .net  error occurs when an alarm/alert should be triggered, the initial alarm/alert will not be delivered until a  subsequent alarm/alert is triggered. At that time, the initial alarm/alert is delivered, but not the second one.  Alarm/alerts will continue to be delayed and be one alarm/alert behind, causing delayed alarm/alerts until the  receiver is reset. This condition could result in the missed detection of a hyperglycemic or hypoglycemic event.  Second, a single EGV reading may be delayed for 5 minutes after the initial .net operating system error. If the  user receives a single EGV reading delayed by 5 minutes, the delay is not expected to cause user harm.",
      "recall_initiation_date": "20250127",
      "center_classification_date": "20250220",
      "report_date": "20250226",
      "code_info": "All Serial Numbers/UDI: 00386270000583"
    }
  ]
}