{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Blue Ash",
      "state": "OH",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92409",
      "recalling_firm": "Megadyne Medical Products, Inc.",
      "address_1": "4545 Creek Rd",
      "address_2": "N/A",
      "postal_code": "45242-2803",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed US Nationwide.",
      "recall_number": "Z-1999-2023",
      "product_description": "MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode.  used during electrosurgery",
      "product_quantity": "21,100 units",
      "reason_for_recall": "Firm has received reports of patient burns in surgical procedures where device was used.",
      "recall_initiation_date": "20230601",
      "center_classification_date": "20230629",
      "report_date": "20230705",
      "code_info": "Model No. 0847; UDI-DI: 10614559104842; All Units.",
      "more_code_info": ""
    }
  ]
}