{
  "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": "Ongoing",
      "city": "Rocklin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88308",
      "recalling_firm": "Ortho8, Inc.",
      "address_1": "2217 Plaza Dr",
      "address_2": "N/A",
      "postal_code": "95765-4421",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of Al, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MO, NC, NV,  NJ, NY, OK, PA, SC, TN, TX, UT, VA.",
      "recall_number": "Z-2325-2021",
      "product_description": "EVEXIA LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF(s): EVE-11/EVE-X11, Rx Only, Not Sterile",
      "product_quantity": "N/A",
      "reason_for_recall": "EVEXIA LUXE DVT PREVENTION DEVICE is marketed without FDA clearance",
      "recall_initiation_date": "20210709",
      "center_classification_date": "20210819",
      "report_date": "20210825",
      "code_info": "All Lots"
    }
  ]
}