DYNAMITE SUPER capsule recall
DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
Why was DYNAMITE SUPER capsule recalled?
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with 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?
The recall is ongoing. Follow the firm and FDA 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/Item#: OMS760-B, Exp: 12/2025
- Product
- DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
- Recalling firm
- Gadget Island, Inc
- Quantity
- 140 blister packs
- Distribution
- Nationwide in the USA.
- Recall date
- May 10, 2023
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)