Junp Hydration LLC 2022-02-16 Health critical FDA
Health · FDA · Recall #FDA-D-0557-2022
MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a… Recall
Issued February 16, 2022 · Junp Hydration LLC
In February 2022, Junp Hydration LLC recalled the MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a…, 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: product was found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
What you should do
- 1 Stop using MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Junp Hydration LLC 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
- Junp Hydration LLC
- Category
- Health
- Recall date
- February 16, 2022
- Units affected
- Not reported
- Sold at
- Product was distributed nationwide in the USA via Amazon Marketplace
- Recall number
- FDA-D-0557-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Junp Hydration LLC has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.