{
  "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": "Middleton",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93969",
      "recalling_firm": "Natus Neurology Inc",
      "address_1": "3150 Pleasant View Rd",
      "address_2": "",
      "postal_code": "53562-4800",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Canada.",
      "recall_number": "Z-1305-2024",
      "product_description": "TENSIVE Conductive Adhesive Gel, REF 016-401600",
      "product_quantity": "80 units",
      "reason_for_recall": "Natus has become aware that its third-party supplier Parker Laboratories Inc. is conducting a voluntary recall related to their Tensive Conductive Adhesive Gel, Ref. 22-60 Lot Number A0623009. They have received five complaints. These customers reported that the gel is too thick, is discolored (darker than usual), and in one instance, patients reported irritation after procedures using the gel.",
      "recall_initiation_date": "20240207",
      "center_classification_date": "20240319",
      "report_date": "20240327",
      "code_info": "UDI/DI 00855683006333, Lot Numbers:  A0623009",
      "more_code_info": ""
    }
  ]
}