{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "43531",
      "product_res_number": "Z-0473-06",
      "event_date_initiated": "2005-12-30",
      "event_date_posted": "2006-02-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-08-24",
      "res_event_number": "34322",
      "product_code": "LPD",
      "pma_numbers": [
        "P980003"
      ],
      "product_description": "Chilli II Cooled Ablation Cathether, Model M00490310",
      "code_info": "Batch Numbers: 804828 and 8048029",
      "firm_fei_number": "3001236349",
      "recalling_firm": "Boston Scientific Corp",
      "address_1": "2710 Orchard Pkwy",
      "city": "San Jose",
      "state": "CA",
      "postal_code": "95134",
      "additional_info_contact": "Deborah Springer\n408-895-3626",
      "reason_for_recall": "Product is mislabeled with the incorrect catheter curve description.",
      "root_cause_description": "Other",
      "action": "On 12/30/05, the firm issued letters via Federal Express to all its direct consignees, informing them of the affected product and providing instructions on the recall.",
      "product_quantity": "35 units",
      "distribution_pattern": "Product was released for distribution to 14 consignees in US.",
      "openfda": {}
    }
  ]
}