{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Campbell",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88334",
      "recalling_firm": "Ostial Corporation",
      "address_1": "197 E Hamilton Ave Ste 101",
      "address_2": "N/A",
      "postal_code": "95008-0261",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, MI, OH, IN, KY, MT, FL, PA, GA, MN, KS, NY, IL, SD, LA, SC, CT.",
      "recall_number": "Z-2309-2021",
      "product_description": "FLASH Ostial System, Dual Balloon Angioplasty Catheter, REF: OAB6014BA",
      "product_quantity": "40",
      "reason_for_recall": "Angioplasty system has a manufacturing issue that has the potential to result in difficulty deflating the outer balloon, which may result in increased risk of access site complications.",
      "recall_initiation_date": "20210714",
      "center_classification_date": "20210817",
      "termination_date": "20240130",
      "report_date": "20210825",
      "code_info": "Lot: 82210399"
    }
  ]
}