{
  "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": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92300",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of OR, SC, VA, TN, GA, NC, CO, NC, FL.",
      "recall_number": "Z-2007-2023",
      "product_description": "NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed",
      "product_quantity": "7 software versions",
      "reason_for_recall": "Baxter identified a potential risk where the \"safety\" monitoring and \"bed exit\" monitoring features may enter a permanent state of alert suppression. In this state, a caregiver may not be alerted remotely when assigned patient protocols (bed exit, siderail position, brakes off, height of bed changes, head of bed angle, and/or turn reminders) are turned off.",
      "recall_initiation_date": "20230519",
      "center_classification_date": "20230626",
      "report_date": "20230705",
      "code_info": "UDI/DI 00887761985193, Software Versions:  3.9: 3.9.200,3.9.201, 3.9.300, 3.9.400, 3.9.401, 3.9.500, 3.9.600",
      "more_code_info": ""
    }
  ]
}