{
  "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": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93567",
      "recalling_firm": "Getinge Usa Sales Inc",
      "address_1": "1 Geoffrey Way",
      "address_2": "N/A",
      "postal_code": "07470-2035",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide. Global Distribution.",
      "recall_number": "Z-0771-2024",
      "product_description": "Maquet Hanaulux 2006/ 2007, Blue 100, Blue 130/ 90, Blue Series 30/ 80, and Prismatic OR Light Systems.  No Model Numbers.",
      "product_quantity": "236793 units in total",
      "reason_for_recall": "A potential for a light system to fall in the operating room.",
      "recall_initiation_date": "20231108",
      "center_classification_date": "20240118",
      "report_date": "20240124",
      "code_info": "All systems affected"
    }
  ]
}