{
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    "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": "2026-04-01",
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      "country": "United States",
      "city": "Woodbridge",
      "address_1": "1413 Dutchess Ln",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: This dietary supplement has been found to contain sildenafil, an FDA approved drug for the treatment of male erectile dysfunction making this an unapproved new drug.",
      "address_2": "",
      "product_quantity": "40,480 blister packs",
      "code_info": "Lot L08108, Exp 06/15",
      "center_classification_date": "20130516",
      "distribution_pattern": "Nationwide",
      "state": "NJ",
      "product_description": "Super Power capsules, Proprietary Blend 570 mg, packaged in 2-count capsules per blister pack, Distributed by: Freedom Trading, NJ 08863, UPC 7 18122 90678 9.",
      "report_date": "20130522",
      "classification": "Class I",
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      "recalling_firm": "D& S Herbals, LLC",
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      "initial_firm_notification": "Press Release",
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      "event_id": "64190",
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      "recall_initiation_date": "20121222",
      "postal_code": "07095-3855",
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