Food Recall Check
Class III · Low risk Terminated Initiated Sep 10, 2019 (7 years ago)

Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets recall

Recalled by Threshold Enterprises Ltd · Scotts Valley, CA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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

Quantity: 1,822 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Alabama Arizona California Colorado Florida Georgia Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Michigan Missouri North Carolina New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Tennessee Texas Utah Washington

FDA's distribution note: 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.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Threshold Enterprises Ltd
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 10, 2019
In FDA report of
Oct 30, 2019
Terminated
Feb 3, 2020
FDA recall number
F-0061-2020 · event 84038
Official record
FDA enforcement report search

Other recalls by Threshold Enterprises Ltd

Class II · Moderate risk Terminated Labeling

Planetary Herbals Mullein Lung Complex

Reason Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inactive ingredients).

Threshold Enterprises Ltd Nationwide F-1097-2019
Class II · Moderate risk Terminated Other

Planetary Herbals Ginseng Classic

Reason Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.

Threshold Enterprises Ltd 7 states F-3338-2017
Class II · Moderate risk Terminated Labeling

Source Naturals Dietary Supplement Vitamin D-3

Reason Testing of Vitamin D-3 as a result of a consumer complaint found specific lots to have lower concentrations than product specifications of ingredient labeling.

Threshold Enterprises Ltd Nationwide F-2178-2017

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