{
  "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": [
    {
      "status": "Terminated",
      "city": "Dublin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63596",
      "recalling_firm": "Carl Zeiss Meditec, Inc.",
      "address_1": "5160 Hacienda Dr",
      "address_2": "N/A",
      "postal_code": "94568-7562",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including IL and MD",
      "recall_number": "Z-0406-2013",
      "product_description": "INTRABEAM Balloon Applicator Set;  4.0 cm,  Carl Zeiss Meditec AG, Oberkochen, Germany    INTRABEAM System is intended for radiation therapy treatments.",
      "product_quantity": "36 total, all lots",
      "reason_for_recall": "A manufacturing defect has been identified which could results in the small tube becoming dislodged between the luer fitting and the check valve.",
      "recall_initiation_date": "20121025",
      "center_classification_date": "20121120",
      "termination_date": "20121120",
      "report_date": "20121128",
      "code_info": "Part number 304534-7500-002; lot number 540960."
    }
  ]
}