{
  "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": "91112",
      "recalling_firm": "DeVilbiss Healthcare LLC",
      "address_1": "100 Devilbiss Dr",
      "address_2": "",
      "postal_code": "15501-2125",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide. Foreign distribution pending.",
      "recall_number": "Z-0724-2023",
      "product_description": "DeVilbiss, 525 5-liter Oxygen Concentrator  Models 525DS, 525DS-Q",
      "product_quantity": "1004315 (US); 414559 (OUS)",
      "reason_for_recall": "The firm has received complaints of the device becoming hot. The firm has updated the user manual to include warnings that applied parts in contact with the patient may in some situations exceed 41 degrees Celsius (105.8 degrees Fahrenheit), clarification on expected service life, and the need for maintenance to certain components.",
      "recall_initiation_date": "20221118",
      "center_classification_date": "20221219",
      "report_date": "20221228",
      "code_info": "Model 525DS UDI-DI 00885304000846 All Lots  Model 525DS-Q UDI-DI 00885304009689 All Lots",
      "more_code_info": ""
    }
  ]
}