{
  "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": "Toano",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97149",
      "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": "Domestic: CA, IL, MD, OH, PA, TX, WA.",
      "recall_number": "Z-2259-2025",
      "product_description": "PACK GENERAL ROBOTIC. Medical convenience kit.",
      "product_quantity": "656 units",
      "reason_for_recall": "CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.",
      "recall_initiation_date": "20250611",
      "center_classification_date": "20250804",
      "report_date": "20250813",
      "code_info": "Model No. RDLD047-10; UDI: 10809160358603; Kit Lot No. 1589630, 1590570, 1610157, 1617028, 1618142, 1621537, 1629589, 1635288, 1636852.",
      "more_code_info": ""
    }
  ]
}