{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "210374",
      "product_res_number": "Z-0329-2025",
      "event_date_initiated": "2022-07-11",
      "event_date_posted": "2024-11-08",
      "recall_status": "Open, Classified",
      "res_event_number": "95490",
      "product_code": "LLI",
      "product_description": "SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers:  01-011539, 01-011541, 01-01198",
      "code_info": "UDI/DI 4050621100401, 19-0990\nUDI/DI 4050621100012, 19-1062\nUDI/DI 4050621100432, 19-1152\nUDI/DI 4050621100449, 19-1119\nUDI/DI 4050621100470, 19-1155\nUDI/DI 4050621100487, 19-1156",
      "firm_fei_number": "3015979371",
      "recalling_firm": "WISSNER-BOSSERHOFF GMBH",
      "address_1": "Hauptstr. 4-6 4-6 hauptstr.",
      "city": "Wickede Ruhr",
      "country": "Germany",
      "reason_for_recall": "When the handset is disconnected from the power mains, and mains operation is restored, the handset is reset to the preset Resident mode. In this mode, the backrest, legrest, and height adjustment can be moved.",
      "root_cause_description": "Device Design",
      "action": "Wissner-bosserhoff issued an Urgent safety information notice along with supplement use instructions notice to its sole US consignee on 07/11/2022. The notice explained the problem, risk to patient, and requested the user update the IFU for the device.  Distributors were directed to notify their customers.",
      "product_quantity": "77 units",
      "distribution_pattern": "US Nationwide distribution in the states of NC.",
      "openfda": {
        "k_number": [
          "K840787",
          "K022387"
        ],
        "registration_number": [
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          "3003749961"
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        "device_name": "Bed, Therapeutic, Ac-Powered, Adjustable Home-Use",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5100",
        "device_class": "2"
      }
    }
  ]
}