{
  "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": "2026-08-13",
    "results": {
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      "event_date_initiated": "2005-11-09",
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      "firm_fei_number": "1823260",
      "recalling_firm": "Roche Diagnostics Corp.",
      "address_1": "9115 Hague Rd",
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      "state": "IN",
      "postal_code": "46256-1025",
      "additional_info_contact": "800-858-8072",
      "reason_for_recall": "Incorrect patient blood glucose test results may be reported due to a software problem.",
      "root_cause_description": "Other",
      "action": "Notification letters dated 11/9/05 were issued to Users, Mail Order Distributors, Clinical Trial Sponsors, Pharmacists and Health Care Professionals.  Press release issued 1/17/06.",
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