{
  "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": "2026-09-17",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "218989",
      "product_res_number": "Z-1809-2026",
      "event_date_initiated": "2025-08-13",
      "event_date_posted": "2026-04-10",
      "recall_status": "Open, Classified",
      "res_event_number": "98528",
      "product_code": "QFG",
      "k_numbers": [
        "K231485",
        "K232224"
      ],
      "product_description": "iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software",
      "code_info": "ILet Ace Pumps containing software version BOM000036 Rev C (version 1.4.2) or older.",
      "firm_fei_number": "3019004087",
      "recalling_firm": "Beta Bionics, Inc.",
      "address_1": "11 Hughes",
      "city": "Irvine",
      "state": "CA",
      "postal_code": "92618-1902",
      "additional_info_contact": "Karen Hynes\n855-745-3800",
      "reason_for_recall": "it was found that in versions 1.3.7, 1.4.2, and 1.4.3, the Lock Screen and Limited Access Passcode Screen on the iLet graphical user interface (GUI) include certain icons displayed in the status bar that are active, thereby allowing the user to bypass those screens when those icons on the status bar are pressed, allowing unauthorized access while the device is in Limited Access Mode. A Health Risk associated with Limited access mode includes severe hypoglycemia due to unauthorized access to the iLet if someone were to make unauthorized meal announcements or stopped insulin delivery.",
      "root_cause_description": "Software design",
      "action": "On March 12, 2026 Beta Bionics issued a  Urgent  Medical Device Correction - Expansion/Update via Email to notify new consignees and previous consignees. Initial notification was issued on August 13, 2025. Beta Bionics ask consignees to take the following actions:\n\n1. Download or update your iLet app on your phone.  Read the iLet App User Guide.\n2. Log into your iLet app.\n3. Position your iLet next to your phone with the app open.\n4. Go to app settings on the iLet app and follow the on-screen instructions to update to the latest firmware.\n5. Complete the acknowledgment survey https://sprw.io/stt-6HnQU or scan the\nQR code. This survey helps us monitor the effectiveness of the recall action.",
      "product_quantity": "15 units",
      "distribution_pattern": "US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, LA, MA, MD, ME, MI, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WY AND WASHINGTON DC.",
      "openfda": {
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          "K253976",
          "K191679",
          "K203768",
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          "K250792",
          "DEN180058",
          "K213134",
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          "K253743",
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          "K223213",
          "K253470",
          "K232380",
          "K203234",
          "K201214",
          "K252770",
          "K233044"
        ],
        "device_name": "Alternate Controller Enabled Insulin Infusion Pump",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "880.5730",
        "device_class": "2",
        "registration_number": [
          "2022435",
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