{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Van Nuys",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92389",
      "recalling_firm": "Appliedvr",
      "address_1": "16760 Stagg St Ste 216",
      "address_2": "N/A",
      "postal_code": "91406-1642",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: NY OUS: None",
      "recall_number": "Z-2044-2023",
      "product_description": "RelieVR REF: RVX-2002, Rx Only.  Virtual reality behavioral therapy device for pain relief.",
      "product_quantity": "1 unit",
      "reason_for_recall": "There is the potential for the program software to malfunction which will not allow it to move forward to the next session.",
      "recall_initiation_date": "20230227",
      "center_classification_date": "20230629",
      "report_date": "20230705",
      "code_info": "Serial Number: PA7940RGG5130514B; UDI: 0100850038247027211001077",
      "more_code_info": ""
    }
  ]
}