{
  "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": {
      "skip": 0,
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  "results": [
    {
      "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-0300-2024",
      "product_description": "Target brand High Performance Lubricant Eye Drops (Polyethylene glycol 400 0.4%, Propylene glycol 0.3%) a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 11673-522-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 11673-522-30), Distributed by: Target Corporation Minneapolis, MN 55403",
      "product_quantity": "401,568 bottles",
      "reason_for_recall": "Non-Sterility",
      "recall_initiation_date": "20231113",
      "center_classification_date": "20240205",
      "report_date": "20240214",
      "code_info": "All lots",
      "more_code_info": ""
    }
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}