{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Webster",
      "address_1": "253 Medical Center Blvd",
      "reason_for_recall": "There was an error on the outer labeling of this device.  The inner label was correct.",
      "address_2": "",
      "product_quantity": "3",
      "code_info": "Model Number: S-05-100-120-G3;  Lot Number 01049037",
      "center_classification_date": "20130618",
      "distribution_pattern": "Nationwide Distribution to the states of FL, NY, and PA.",
      "state": "TX",
      "product_description": "IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms",
      "report_date": "20130626",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "IDEV Technologies, Inc.",
      "recall_number": "Z-1550-2013",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "65245",
      "termination_date": "20130729",
      "more_code_info": "",
      "recall_initiation_date": "20120529",
      "postal_code": "77598-4213",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}