Pyramids Wholesale recalls libigrow RED DRAGON+ Maximum Strength Formula due to undeclared sildenafil and tadalafil. Consumers should stop using the product immediately.
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Pyramids Wholesale is recalling libigrow RED DRAGON+ Maximum Strength Formula capsules because they contain undeclared sildenafil and tadalafil without proper FDA approval. This poses a risk of serious health effects due to unapproved ingredients.
The product contains undeclared sildenafil and/or tadalafil, which are prescription medications not approved by the FDA. Using these unapproved drugs can cause serious health issues like heart problems or interactions with other medications.
Anyone who owns or uses the libigrow RED DRAGON+ Maximum Strength Formula capsules with UPC 7 05105 83073 5. People with heart conditions or those taking other medications may be at higher risk.
Check for the libigrow RED DRAGON+ Maximum Strength Formula, 2 capsules per box, with UPC 7 05105 83073 5. All lots of this product are affected.
Immediately stop using the libigrow RED DRAGON+ Maximum Strength Formula capsules as they contain undeclared sildenafil and tadalafil.
The product contains undeclared sildenafil and/or tadalafil without FDA approval, which can cause serious health risks.
Stop using it immediately and contact Pyramids Wholesale for further instructions.
Yes, using unapproved medications can lead to serious health issues like heart problems or drug interactions.
We’ve drafted a message you can send Pyramids Wholesale to request your refund or repair — edit it as you like.
Subject: Recall D-0454-2024 — Pyramids Wholesale Pyramids Wholesale Hello, I own a Pyramids Wholesale that is covered by recall D-0454-2024 from Pyramids Wholesale. 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.