{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "29801",
      "product_res_number": "Z-0002-04",
      "event_date_initiated": "2003-08-20",
      "event_date_posted": "2003-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-11-21",
      "res_event_number": "27393",
      "product_code": "GBR",
      "product_description": "Opti-Plast Balloon Dilatation Catheters",
      "code_info": "Models:  XT75410, XT100410, XT120410",
      "firm_fei_number": "2020394",
      "recalling_firm": "Bard Peripheral Vascular Inc",
      "address_1": "1625 W 3rd St",
      "city": "Tempe",
      "state": "AZ",
      "postal_code": "85281-2438",
      "additional_info_contact": "Mary Edwards\n480-303-2640",
      "reason_for_recall": "Product intended for distribution outside USA was distributed without premarket notification requirements being met.",
      "root_cause_description": "Other",
      "action": "The firm notified territory managers by telephone on August 20, 2003 to hold all consigned devices for return.",
      "product_quantity": "14 units",
      "distribution_pattern": "OH, AL, MS, LA, VA",
      "openfda": {}
    }
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}