{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Columbia",
      "address_1": "9176 Red Branch Rd",
      "reason_for_recall": "One bolt on the V motor was not fully tightened which caused a drift of .13 degrees in alignment resulting in reduced dose output.",
      "address_2": "Ste O",
      "product_quantity": "2",
      "code_info": "Serial Numbers GP0002, GP0004;  UDI: (01) 00850002615005",
      "center_classification_date": "20190725",
      "distribution_pattern": "The products were distributed to the following US states:  MD and TX.",
      "state": "MD",
      "product_description": "GammaPod Stereotactic Radiotherapy System Model A, REF XMSGP030A00-0.02    Product Usage:  GammaPod  is a teletherapy device intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.",
      "report_date": "20190731",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Xcision Medical Systems, LLC",
      "recall_number": "Z-2081-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83342",
      "termination_date": "20210701",
      "recall_initiation_date": "20190703",
      "postal_code": "21045-2001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}