Food recall

Threshold Enterprises Ltd recall: Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets

Threshold Enterprises Ltd, of Scotts Valley, CA, recalled Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets. The FDA's reason: “Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on September 10, 2019, and the FDA first listed it in its Enforcement Report of October 30, 2019. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class III

It is unlikely to cause harm

Why

Labeling, packaging or manufacturing problems

Status

Terminated

Closed February 3, 2020

The recall

Company
Threshold Enterprises Ltd (Scotts Valley, CA)
Reason, in FDA's words
“Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.”
Where it was sold
U.S. distribution to the following: AL, AZ, CA, CO, FL, GA, IL, IN, KS, KY, LA, MA, MD, MI, MO, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, WA No foreign distribution.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
84038

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0061-2020 Class III

    Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets, 60 tablets Manufactured for: Source Natural, Inc. PO Box 2118 Santa Cruz, CA 95062 Item Code: SN2613, SN2614 Item UPC: 021078026136, 021078026143

    Codes: Lot Number: FG-99741, FG-100206, FG-99742, FG-100207

    Quantity: 1,822 bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of October 30, 2019.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.