{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Dongguan",
      "state": "",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81973",
      "recalling_firm": "BrosMed Medical Co.,Ltd.",
      "address_1": "Bubugaogaofu Lou Lou 15th",
      "address_2": "Songshan Lake Hi",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to MO.",
      "recall_number": "Z-0963-2019",
      "product_description": "Hermes NC PTA Balloon Dilatation Catheter    The balloon dilatation catheter is intended to dilate stenoses in the iliac, femoral, iliofemoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This device is also indicated for stent dilatation post-deployment in the peripheral vasculature.",
      "product_quantity": "400",
      "reason_for_recall": "Incorrect (higher) Rated Burst Pressure information printed on label.",
      "recall_initiation_date": "20181214",
      "center_classification_date": "20190227",
      "termination_date": "20201211",
      "report_date": "20190306",
      "code_info": "Lot #'s: F1800580, F1800582, F1800583, F1800585, F1800581, F1800584, F1804186, F1804187, F1804188, and F1804189.",
      "more_code_info": ""
    }
  ]
}