{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Glenwood",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93524",
      "recalling_firm": "Landauer",
      "address_1": "2 Science Rd",
      "address_2": "",
      "postal_code": "60425-1531",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US and Australia, Brazil, Canada, China, France, Germany, India, Japan, Mexico, Rep of Korea, Taiwan, Thailand, Viet Nam",
      "recall_number": "Z-0616-2024",
      "product_description": "Landauer microSTARii reader, Medical Dosimetry System, Model Numbers:  18000-000/18001-000/18007-000",
      "product_quantity": "584 units",
      "reason_for_recall": "MicroSTARii readers may be contributing to the nanodot dosimeter measurement inaccuracy in two possible ways. The first is related to the interaction of the reader s LED beam profile with the nanoDot dosimeter. The second is debris formation due to drawer actuation, resulting in a change of reader response that may not be detectable unless known dose QCs are being run regularly.",
      "recall_initiation_date": "20231115",
      "center_classification_date": "20231222",
      "report_date": "20240103",
      "code_info": "All serial numbers.",
      "more_code_info": ""
    }
  ]
}