{
  "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": "Charlottesville",
      "address_1": "700 Harris St Ste 109",
      "reason_for_recall": "Segmented cylinder applicator set may slip during treatment, causing the delivery of radiation to areas outside the target.",
      "address_2": "",
      "product_quantity": "21 devices",
      "code_info": "Serial numbers H640383, H640277, H640384, H640788, H640D126, H640385, H640372, H640303, H640387",
      "center_classification_date": "20130514",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) and in the countries of: Belgium, France, Martinique, Slovenia, Sweden, and the United Kingdom.",
      "state": "VA",
      "product_description": "Segmented Cylinder Applicator Set, Model # GM11004150, when used for Pulsed Dose Rate (PDR)    Product Usage:  Usage:  Used during pulsed dose rate brachytherapy to treat vaginal and rectal cancer.",
      "report_date": "20130522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Varian Medical Systems, Inc.",
      "recall_number": "Z-1324-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64986",
      "termination_date": "20140113",
      "more_code_info": "",
      "recall_initiation_date": "20130411",
      "postal_code": "22903-4584",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}