{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sunnyvale",
      "address_1": "100 Mathilda Pl",
      "reason_for_recall": "A drug strength in MOSAIQ can be changed during the ordering process and approved, but the saved drug strength reverts to the original value.",
      "address_2": "5th Floor",
      "product_quantity": "31",
      "code_info": "MOSAIQ 2.83 when run with First Data Bank (FDB), UDI/GTIN MOSAIQ 2.83 (0858164002367)",
      "center_classification_date": "20210929",
      "distribution_pattern": "Distribution was made to CA, CO, FL, ID, LA, MO, MS, NC, NH, NM, NV, NY, OH, OK, PA, SD, and WA.  There was no military/government distribution.    Foreign distribution was made to Australia, Canada, and the United Kingdom.",
      "state": "CA",
      "product_description": "MOSAIQ Oncology Information System",
      "report_date": "20211006",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-2591-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "88599",
      "recall_initiation_date": "20210902",
      "postal_code": "94086-6076",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}