RecallHawk
Class II Recall

Brain MD - Brain & Memory Power Boost Supports Healthy Brain and Memory Performance 120 capsules - Dietary Supplement U

BRAINMD

Summary

The FDA issued a Class II for Brain MD - Brain & Memory Power Boost Supports Healthy Brain and Memory Performa by BRAINMD. Reason: It was discovered that bottles of Brain and Memory Power Boost was filled with multi vitamin-mineral product - NeuroVite Plus.

Details

Source

Food Recall

External ID

F-0010-2022

Action Date

2021-10-13

Status

Terminated

Category

food

Product Description

Brain MD - Brain & Memory Power Boost Supports Healthy Brain and Memory Performance 120 capsules - Dietary Supplement UPC: 8 57568 00341 3 Serving Size - 4 capsules' Servings per container - 30 Ingredients - amount per serving: Phosphatidylserine (PS) - 100 mg Acetylcarnitine - 666 mg N-Acetylcysteine (NAC) - 400 mg Alpha-Lipoic Acie - 200 mg Ginkgo Biloba - 121- mg Huperzine A - 100 mcg Other ingredients: Vegetable cellulose, silicon dioxide, magnesium stearate, microcrystalline cellulose. Developed and distributed by: BrainMD, Irvine, CA; brainmd.com

Lot/Code Info: Lot No. N21301001, Best By 10/1/2022, sku 83-N

Quantity Affected: 1,765 units/bottles

Reason for Recall

It was discovered that bottles of Brain and Memory Power Boost was filled with multi vitamin-mineral product - NeuroVite Plus

Distribution

Direct sales from firm's web site

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-09

Company

BRAINMD

Irvine, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 23 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (BRAINMD) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does BRAINMD have FDA actions?

This is the only FDA action we have on record for BRAINMD in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0010-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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