{
  "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": "Ra'Anana",
      "state": "",
      "country": "Israel",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97463",
      "recalling_firm": "CORNEAT VISION, LTD.",
      "address_1": "4, Ha-Sheizaf",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AZ, CA, CO, CT, DC, DE, FL, GA, ID, \tIL, IN, KS, MA, MD, MI, MN, MO, MT, NC, NY, OH, PA, SC, TN, TX, UT, VA, WA, WI and the countries of Japan, Israel, Argentina, Hong Kong.",
      "recall_number": "Z-0039-2026",
      "product_description": "CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m",
      "product_quantity": "630 units",
      "reason_for_recall": "Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.",
      "recall_initiation_date": "20250818",
      "center_classification_date": "20251003",
      "report_date": "20251015",
      "code_info": "All Lots/ UDI: G16010362950",
      "more_code_info": ""
    }
  ]
}