{
  "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": "Saratoga",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85532",
      "recalling_firm": "Capso Vision, Inc.",
      "address_1": "18805 Cox Ave Ste 250",
      "address_2": "N/A",
      "postal_code": "95070-6615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution including in the states of FL, GA, NY, PA, and TX.",
      "recall_number": "Z-2073-2020",
      "product_description": "CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The CapsoCam Plus video capsule system is intended for visualization of the small bowel mucosa in adults. It may be used as a tool in the detection of abnormalities of the small bowel.",
      "product_quantity": "44 units",
      "reason_for_recall": "Possible mis-labeling of the device with incorrect serial number labels which may result in a patient's misdiagnosis.",
      "recall_initiation_date": "20190703",
      "center_classification_date": "20200521",
      "termination_date": "20210128",
      "report_date": "20200527",
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