{
  "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,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Wuxi",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "96210",
      "recalling_firm": "Wuxi Medical lnstrument Factory Co., Ltd.",
      "address_1": "D, Zhangjing",
      "address_2": "No. 43 Xixin Road; Xibeizhen Xishan",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL",
      "recall_number": "D-0247-2025",
      "product_description": "ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per Carton, Sterile, Manufactured by Wuxi Medical Instrument Factory Co., Ltd., Made in China, Manufactured for: Rece International Corp., Miami Lakes, FL, 33014, USA, NDC: 70006-500-01.",
      "product_quantity": "37,500 Boxes",
      "reason_for_recall": "Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.",
      "recall_initiation_date": "20250212",
      "center_classification_date": "20250221",
      "report_date": "20250305",
      "code_info": "Lot #s: 200830, Exp 08/29/2025; 210925, Exp 09/24/2026; 221225, Exp 12/24/2027."
    }
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}