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

Recall #D-0557-2022 Date: February 4, 2022 Classification: Class I Status: Terminated

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.

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