{
  "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": "Sunnyvale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95832",
      "recalling_firm": "Aerin Medical, Inc.",
      "address_1": "232 E Caribbean Dr",
      "address_2": "",
      "postal_code": "94089-1007",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution: AL, AZ, CA, CO, GA, ID, IL, IN, KY LA, MI, MN, NY, NE, NY, OH, OR PA, SC, TN, TX, UT, VA, WA, WI, and WV.",
      "recall_number": "Z-0808-2025",
      "product_description": "Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.",
      "product_quantity": "479 units",
      "reason_for_recall": "Some units in a single production lot were programmed incorrectly which will result in the VivAer Stylus being incorrectly recognized as RhinAer Stylus when connected to the Aerin Console.",
      "recall_initiation_date": "20241112",
      "center_classification_date": "20250106",
      "report_date": "20250115",
      "code_info": "Lot #10235, exp. 2026-05-01; UDI (01)08886479300269(17)260501(10)10235",
      "more_code_info": ""
    }
  ]
}