{
  "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": "2026-09-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 6
    }
  },
  "results": [
    {
      "cfres_id": "217825",
      "product_res_number": "Z-1011-2026",
      "event_date_initiated": "2025-11-26",
      "event_date_posted": "2026-01-16",
      "recall_status": "Open, Classified",
      "res_event_number": "98185",
      "product_code": "LLI",
      "product_description": "MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4",
      "code_info": "1) UDI/DI 40080196320999, All lots; 2) UDI/DI 40080196320999, All Lots",
      "firm_fei_number": "1417592",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "city": "Northfield",
      "state": "IL",
      "postal_code": "60093-2753",
      "additional_info_contact": "Haley Barclay\n866-359-1704",
      "reason_for_recall": "Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire.\nMedline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.",
      "root_cause_description": "Device Design",
      "action": "Medline issued an URGENT MEDICAL DEVICE RECALL notice with an enclosed URGENT MEDICAL DEVICE FIELD CORRECTION NOTICE to its consignees on 11/26/2025 via email and USPS first class mail. The notice explained the issue, potential risks, and requested the user ONLY USE MEDLINE SIDE RAILS and MEDLINE ACCESSORIES that are intended for use with Medline Homecare Beds. When using Medline Side Rails and Medline Accessories, follow all applicable instructions for use.  \nDistributors were directed to notify their customers. For questions, contact the Recall Department at 866-359-1704 orrecalls@medline.com.",
      "product_quantity": "373392 units",
      "distribution_pattern": "US, CA, PA, GUAM, VI",
      "openfda": {
        "k_number": [
          "K022387",
          "K840787"
        ],
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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"
      }
    }
  ]
}