FDAFDA · Food and drugs·Recall number D-0638-2022
RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.
Published February 23, 2022 · Recall initiated: February 8, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Celebrate Today
- Distributor
- Product was distributed nationwide in the USA via Amazon Marketplace
- Lot
- Lot # DK1027, Exp. 08/01/2023
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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