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| FDA Recalls Recall Information from the US Food and Drug Administration |
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The Menz Club, LLC . Issues a voluntary nationwide recall of V-Maxx Rx due to undeclared sulfoaildenafil An FDA lab analysis of V Maxx Rx Lot # 101109 distributed by The Menz Club, LLCwas found to contain undeclared sulfoaidenafil. Sulfoaidenafil is an analog of sildenafil,an FDA approved prescription drug used to treat Erectile Dysfunction (ED), making VMaxx Rx, an unapproved new drug. |
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