{
  "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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  "results": [
    {
      "status": "Ongoing",
      "city": "Ambarnath",
      "state": "",
      "country": "India",
      "classification": "Class II",
      "openfda": {
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        ],
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        "product_type": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "94542",
      "recalling_firm": "Rubicon Research Private Limited",
      "address_1": "4 & K30 5 Plot No K - 30",
      "address_2": "District",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0517-2024",
      "product_description": "Metoprolol Tartrate Tablets USP, 25mg, 1000 count bottle, Rx only, distributed by: TruPharma, LLC, Tampa, FL 33609, Manufactured by: Rubicon Research Private Limited, Ambernath Dist Thane 421506 India, NDC 52817-360-00",
      "product_quantity": "11,664 Bottles",
      "reason_for_recall": "Presence of Foreign Substance: metal in tablet",
      "recall_initiation_date": "20240506",
      "center_classification_date": "20240529",
      "report_date": "20240605",
      "code_info": "Lot 231037H1, exp 6/2027",
      "more_code_info": ""
    }
  ]
}