FDA found undeclared sildenafil in Red Bull Extreme Male Enhancement Supplement. Recall covers 15 pouches per box with May 2024 production date. Consumers should stop using immediately.
FDA analysis revealed the presence of undeclared sildenafil
Pure Vitamins and Natural Supplements, LLC is recalling 15 pouches per box of Red Bull Extreme Male Enhancement Supplement due to FDA-identified undeclared sildenafil. This poses a risk of unintended medication effects as sildenafil is a prescription drug.
The supplement contains sildenafil, a prescription drug for erectile dysfunction, which was not declared on the label. This can lead to unintended medication effects such as side effects from taking a drug without proper medical supervision.
Men who have purchased the Red Bull Extreme Male Enhancement Supplement, which contains undeclared sildenafil, are at risk of unintended medication effects. Those who have consumed the product should stop using it immediately.
Check for the product name 'Red Bull Extreme Male Enhancement Supplement' with 15 pouches per box. The product was produced by Pure Vitamins and Natural Supplements, LLC with a May 2024 manufacturing date and an expiration date of May 2029.
Immediately stop using the recalled supplement as it contains undeclared sildenafil, a prescription drug.
No, the product contains undeclared sildenafil, which is a prescription drug and can cause unintended medication effects.
The recall covers 15 pouches per box of Red Bull Extreme Male Enhancement Supplement.
The product was manufactured in May 2024 with an expiration date of May 2029.
We’ve drafted a message you can send Red Bull to request your refund or repair — edit it as you like.
Subject: Recall H-0655-2026 — Red Bull Red Bull Hello, I own a Red Bull that is covered by recall H-0655-2026 from Red Bull. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
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