{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Toano",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99249",
      "recalling_firm": "AVID Medical, Inc.",
      "address_1": "9000 Westmont Dr",
      "address_2": "N/A",
      "postal_code": "23168-9351",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of California.",
      "recall_number": "Z-2763-2026",
      "product_description": "Halyard EYE PACK. Model/Catalog Number: LVEY27    Convenience kit.",
      "product_quantity": "260 kits",
      "reason_for_recall": "Incorrect concentration of Betadine solution contained within certain AVID convenience kits.",
      "recall_initiation_date": "20260507",
      "center_classification_date": "20260720",
      "report_date": "20260729",
      "code_info": "Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027)."
    }
  ]
}