{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Denver",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94498",
      "recalling_firm": "WAVi Co.",
      "address_1": "3857 N Steele St Ste 1293",
      "address_2": "N/A",
      "postal_code": "80205-4996",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: NC, TX, IL, NV, AZ, NY, CA, MI, KS, AL, FL, MD, UT, WA, PA, GA, AR, NM, CO, IA, CT, IN, VA, LA, HI, MA, OH, OR, MO, KY, ID",
      "recall_number": "Z-1942-2024",
      "product_description": "WAVi Research EEG Desktop System is comprised of the WAVi Research EEG Desktop Software with Instruction Manual and Brochure, and Heart Rate Variability (HRV) Ear Clips. The system kit also incorporates use of the firm's cleared EEG analysis technology (the WAVi SCAN EEG System and Accessories, and the WAVi Headset and eSoc Single Use Electrode Contacts).",
      "product_quantity": "281",
      "reason_for_recall": "Following an FDA-issued Warning Letter, the firm requested return of their research EEG system components due to the closing of their research study.",
      "recall_initiation_date": "20231208",
      "center_classification_date": "20240531",
      "report_date": "20240612",
      "code_info": "Desktop software version 1.0.0.2",
      "more_code_info": ""
    }
  ]
}