{
  "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": "2026-10-13"
  },
  "results": [
    {
      "term": "Adverse Event Without Identified Device or Use Problem",
      "count": 8
    },
    {
      "term": "Patient Data Problem",
      "count": 6
    },
    {
      "term": "Missing Test Results",
      "count": 2
    },
    {
      "term": "Date/Time-Related Software Problem",
      "count": 1
    },
    {
      "term": "Fluid/Blood Leak",
      "count": 1
    },
    {
      "term": "Insufficient Device Problem Information",
      "count": 1
    },
    {
      "term": "Manufacturing, Packaging or Shipping Problem",
      "count": 1
    },
    {
      "term": "No Apparent Adverse Event",
      "count": 1
    },
    {
      "term": "Use of Incorrect Control/Treatment Settings",
      "count": 1
    }
  ]
}