{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84290",
      "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": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0929-2020",
      "product_description": "Dexcom Receiver, REF:  MT22719, (Black, Pin, Blue), Rx Only, containing software version SW10617 and revision 4.0.1.048 - Product Usage: A non-adjunctive invasive glucose sensor is intended to determine glucose levels, and the direction and rate of change of glucose levels in people with diabetes. The device is indicated to replace information obtained from standard blood glucose monitoring devices to make diabetes-related treatment decisions. The device also provides historical glucose information, facilitating long-term therapy adjustments.",
      "product_quantity": "112,415 receivers",
      "reason_for_recall": "It has been reported that use of the mobile receiver with software version SW10617 rev 4.0.1.048 have reported: 1. the receiver becoming stuck on initialization screen when powering on.  This will cause patients not to be able to receive glucose values or alerts; 2. Reinitialization of the receiver without user interaction. If this occurs, the receiver will either reboot and operate normally or require the user to press the Select button on the receiver in order to resume normal operation. In this situation, the user is provided an audio and vibratory alert every 5 minutes. Until the select button is pressed, patients will not receive glucose values or alerts.",
      "recall_initiation_date": "20190712",
      "center_classification_date": "20200131",
      "termination_date": "20221215",
      "report_date": "20200212",
      "code_info": "All  serial numbers of the G5 Mobile Receivers with software version SW10617  and software revision 4.0.1.048    Receiver Part Number/Reciver Kit Number/GUDID registered GTINS/ Receiver Kit Type:    Dexcom G5 Mobile Receiver, MT22179 (BLK) Rev 013 and Rev 014 Receiver (mg/dL), Black   STK-GF-001/ 10386270000238 - Starter Kit  STK-RF-001/20386270000235 - Retail Starter Kit  STR-GF-001/30386270000232 - Replacement Receiver Kit  STK-GF-IUO/NA - Investigational Use  STK-MC-001/00386270000606 - Medicare Starter Kit    Dexcom G5 Mobile Receiver, MT22719 (PNK) Rev 012 and 013, Receiver (mg/dL), Pink  STK-GF-PNK/ 30386270000263 - Starter Kit  STK-RF-PNK/10386270000269 - Retail Starter Kit  STR-GF-PNK/20386270000266 - Replacement Receiver Kit    Dexcom G5 Mobile Receiver, MT22719 (BLU) Rev 012 and 013, Receiver (mg/dL), Blue  STK-GF-BLU/ 30386270000270 - Starter Kit  STK-RF-BLU/10386270000276 - Retail Starter Kit  STR-GF-BLU/20386270000273 - Replacement Receiver Kit"
    }
  ]
}