{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Germering",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93275",
      "recalling_firm": "PATH",
      "address_1": "Landsberger Str. 65",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US States: FL, MO, OH, WI",
      "recall_number": "Z-0404-2024",
      "product_description": "SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S",
      "product_quantity": "1 unit",
      "reason_for_recall": "Affected lots of product may experience technical distortions to a greater extent than expected.",
      "recall_initiation_date": "20230926",
      "center_classification_date": "20231124",
      "report_date": "20231206",
      "code_info": "UDI-DI: 04260223142475;  Serial Numbers: 280117",
      "more_code_info": ""
    }
  ]
}