{
  "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": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97822",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0467-2026",
      "product_description": "Medline Renewal LigaSure Exact, Dissector without Nano-Coating 21cm FT10 SW Version  4.0.1.15 or lower; Electrosurgical Cutting And Coagulation Device",
      "product_quantity": "4226 units",
      "reason_for_recall": "Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.",
      "recall_initiation_date": "20251001",
      "center_classification_date": "20251107",
      "report_date": "20251119",
      "code_info": "UDI/DI 20193489189688 (each), 10193489189681 (case), All Lots",
      "more_code_info": ""
    }
  ]
}