{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "New London",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95909",
      "recalling_firm": "Carwild Corporation",
      "address_1": "3 State Pier Rd",
      "address_2": "",
      "postal_code": "06320-5817",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "IL, FL, SC. PA, AL Foreign: Netherlands",
      "recall_number": "Z-0799-2025",
      "product_description": "Ivalon CELLULOSE SURGICAL SPEAR- Intended To Be Used During  Ophthalmic Surgical Procedures For Fluid Management    Model Number: Q604237",
      "product_quantity": "300 units",
      "reason_for_recall": "Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.",
      "recall_initiation_date": "20241022",
      "center_classification_date": "20250102",
      "report_date": "20250108",
      "code_info": "LOT NUMBER: 24G1739",
      "more_code_info": ""
    }
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}