{
  "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": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Jia Xing",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99813",
      "recalling_firm": "GRI Medical & Electronic Technology Co., Ltd.",
      "address_1": "1805 Honggao Road",
      "address_2": "Nanhu District",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of MS.",
      "recall_number": "Z-0077-2027",
      "product_description": "HALYARD Laparoscopy Comprehensive Pack II  REF: 49332",
      "product_quantity": "396 kits",
      "reason_for_recall": "Laparoscopy packs labeled as \"latex free\" were found to contain a latex urethral catheter",
      "recall_initiation_date": "20260826",
      "center_classification_date": "20261002",
      "report_date": "20261014",
      "code_info": "UDI-DI: 10680651493320 (unit level), 30680651493324 (case level) Lot Numbers: GL25271CXA-Expiry Date: 2029/3/30; GL25296CXA-Expiry Date: 2029/3/30; GL26076CXA-Expiry Date: 2029/5/31"
    }
  ]
}