{
  "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": "Ventura",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94931",
      "recalling_firm": "Neurovision Medical Products Inc",
      "address_1": "353 San Jon Rd",
      "address_2": "",
      "postal_code": "93001-3250",
      "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-2719-2024",
      "product_description": "Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO",
      "product_quantity": "5 BOXES (25 single kits)",
      "reason_for_recall": "mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.",
      "recall_initiation_date": "20240701",
      "center_classification_date": "20240823",
      "report_date": "20240904",
      "code_info": "LOT: 051724B/ UDI: B006LTE7003PS52",
      "more_code_info": ""
    }
  ]
}