Pyramids Wholesale recalls Flower Power CBD Female Enhancement bottles due to undeclared sildenafil and tadalafil. Products marketed without FDA approval may pose health risks.
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Pyramids Wholesale is recalling Flower Power CBD Female Enhancement products because they contain undeclared sildenafil and tadalafil without FDA approval. This could lead to health risks if used without proper medical oversight.
These products contain undeclared sildenafil and tadalafil, which are prescription medications for erectile dysfunction and pulmonary hypertension. Using them without FDA approval could lead to serious health issues due to improper dosing or interactions with other medications.
Anyone who purchased Flower Power CBD Female Enhancement products from Pyramids Wholesale. Those with underlying health conditions or who use these products without medical supervision are at higher risk.
Check for the 59 ml bottle labeled 'Flower Power, CBD infused Female Enhancement' with UPC 0 678741 351646. All lots are affected.
Verify the product label for the 59 ml bottle with UPC 0 678741 351646.
The products contain undeclared sildenafil and tadalafil without FDA approval, which could pose health risks.
Yes, using these products without FDA approval may lead to serious health issues due to improper dosing or interactions with other medications.
Look for the 59 ml bottle labeled 'Flower Power, CBD infused Female Enhancement' with UPC 0 678741 351646.
We’ve drafted a message you can send Pyramids Wholesale to request your refund or repair — edit it as you like.
Subject: Recall D-0450-2024 — Pyramids Wholesale Pyramids Wholesale Hello, I own a Pyramids Wholesale that is covered by recall D-0450-2024 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.
