RED MAMMOTH capsules recall
RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.
Why was RED MAMMOTH capsules recalled?
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 should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # DK1027, Exp. 08/01/2023
- Product
- RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.
- Recalling firm
- Celebrate Today
- Quantity
- 500 cartons
- Distribution
- Product was distributed nationwide in the USA via Amazon Marketplace
- Recall date
- February 23, 2022
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)