{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Miami",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98922",
      "recalling_firm": "INSPIREMD Inc",
      "address_1": "6303 Waterford District Dr Ste 215",
      "address_2": "N/A",
      "postal_code": "33126-6004",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of AR, AZ, CA, DC, FL, GA, HI, IL, IN, KS, MA, MD, MI, MO, NC, NJ, NV, NY, OH, OR, RI, SD, TN, TX, VA, WA, WI, WV.",
      "recall_number": "Z-2326-2026",
      "product_description": "Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm  Model/Catalog Number: CND0840",
      "product_quantity": "424 units",
      "reason_for_recall": "Stent delivery system may encounter complications during deployment which may result in high resistance  or inability to deploy the stent.",
      "recall_initiation_date": "20260501",
      "center_classification_date": "20260605",
      "report_date": "20260617",
      "code_info": "UDI: 07290120281707; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026"
    }
  ]
}