Gadget Island, Inc 2023-05-10 Health critical FDA
Health · FDA · Recall #FDA-D-0573-2023
DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799… Recall
Issued May 10, 2023 · Gadget Island, Inc
In May 2023, Gadget Island, Inc recalled the DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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 you should do
- 1 Stop using DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Gadget Island, Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Gadget Island, Inc
- Category
- Health
- Recall date
- May 10, 2023
- Units affected
- Not reported
- Sold at
- Nationwide in the USA.
- Recall number
- FDA-D-0573-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Gadget Island, Inc has 2 recalls in our database, including 2 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.