{
  "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": "2026-07-22",
    "results": {
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      "status": "Ongoing",
      "city": "Navi Mumbai",
      "state": "",
      "country": "India",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "93357",
      "recalling_firm": "Kilitch Healthcare India Limited",
      "address_1": "R - 904 905 T T C Industrial Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0311-2024",
      "product_description": "Up&Up brand dry eye relief (Carboxymethylcellulose 0.5%) packaged in 0.5 FL OZ (15 mL) each bottles (Twin Pack), Distributed by: Target Corporation Minneapolis, MN 55403, NDC 76168-800-30",
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      "reason_for_recall": "Non-Sterility",
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      "center_classification_date": "20240205",
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      "code_info": "All lots",
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}