{
  "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": "Ongoing",
      "city": "Somerset",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91804",
      "recalling_firm": "DeVilbiss Healthcare LLC",
      "address_1": "100 Devilbiss Dr",
      "address_2": "",
      "postal_code": "15501-2125",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "Worldwide - US Nationwide distribution.",
      "recall_number": "Z-1558-2023",
      "product_description": "DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR, Model Numbers 1025DS, 1025UK, 1025KS, and 1025KS-AR",
      "product_quantity": "143,397 units",
      "reason_for_recall": "The instruction manual is being replaced with an updated version that is in alignment with labeling requirements specified in the IEC-60101-1 standard.",
      "recall_initiation_date": "20230309",
      "center_classification_date": "20230504",
      "report_date": "20230510",
      "code_info": "Model 1025DS - UDI-DI: 00885304000846; Serial Numbers A175230001DS to A232160185DS;  Model 1025UK - UDI-DI: 00885304022480; Serial Numbers A179210001US to A232060432US;  Model 1025KS - UDI-DI: 00853040224734; Serial Numbers A176060001KS to A232220085KS;  Model 1025KS-AR - UDI-DI: 00853040224734; Serial Numbers A216240003KS to A229210010KR",
      "more_code_info": ""
    }
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}