{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25880",
      "product_res_number": "Z-0603-03",
      "event_date_initiated": "2003-01-08",
      "event_date_posted": "2003-02-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-05-03",
      "res_event_number": "25401",
      "product_description": "Bard Orbiter PV Steerable Catheter\nItem #: 320100 (Marketed in Europe Only)",
      "code_info": "All lot numbers were the 4th digit contains the letter A through M. Ex. 07A''A''1234",
      "firm_fei_number": "1000120754",
      "recalling_firm": "C. R.Bard, Inc./Electrophysiology Division",
      "address_1": "129 Concord Road",
      "city": "Billerica",
      "state": "MA",
      "postal_code": "01821",
      "additional_info_contact": "Chris O. Fappiano\n978-323-2230",
      "reason_for_recall": "Sterile barrier maybe perforated compromising sterility of the device",
      "root_cause_description": "Packaging process control",
      "action": "Bard Electrophysiology notified direct accounts by letter on 1.08.03 via Fed''X. Accounts are requested to return product.",
      "product_quantity": "12 units",
      "distribution_pattern": "Nationwide",
      "openfda": {}
    }
  ]
}