{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99827",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama.",
      "recall_number": "Z-3228-2026",
      "product_description": "Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories    MDR107000P\tBED, MANUAL, MEDLITE",
      "product_quantity": "771,127 total",
      "reason_for_recall": "Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.",
      "recall_initiation_date": "20260814",
      "center_classification_date": "20260930",
      "report_date": "20261007",
      "code_info": "MDR107000P UDI-DI 00080196288284  All lots",
      "more_code_info": ""
    }
  ]
}