MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a carton, ...
FDA Recall #D-0557-2022 — Class I — February 4, 2022
Product Description
MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a carton, UPC 8 48998 00091 2, ASIN B08Z74KS88
Reason for Recall
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.
Recalling Firm
Junp Hydration LLC — Brooklyn, NY
Classification
Class I — Reasonable probability of serious adverse health consequences or death.
Product Type
Drugs
Product Quantity
750 cartons
Distribution
Product was distributed nationwide in the USA via Amazon Marketplace
Code Information
Lot # 2010291, Exp 01/07/2024
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated
What Should You Do?
Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.