Food Recall Check
Class III · Low risk Terminated Initiated May 5, 2022 (4 years ago)

SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMENTS NO SOY recall

Recalled by 6174 Industries, LLC · Huntersville, NC, United States

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

Why it was recalled

Product was labeled as "gluten free" and it may contain gluten.

Undeclared allergen: Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMENTS NO SOY, NO GLUTEN, NO EGGS, NO DIARY, NO NUTS, NO GELATIN, NO ARTIFICIAL COLOR, FLAVOR OR SWEETENER, NO PRESERVATIVES. Dist. & Sold Exclusively By: SuppleBears 14311 Reese Blvd STE Huntersville, North Carolina

Quantity: 62cases/50 bottles/60 gummies per bottle

Food: Eggs Chocolate & candy 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 #392759

Where it was sold

Arkansas Idaho Illinois Michigan New Hampshire Nevada New York Texas

FDA's distribution note: Product was shipped to the following states: AR, ID, IL, MI, NH, NV, NY, & TX.

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. The risk from an undeclared allergen is to people allergic to wheat; for anyone else the product is generally not a safety concern. 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
6174 Industries, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 5, 2022
In FDA report of
Jun 15, 2022
Terminated
Jul 28, 2022
FDA recall number
F-1154-2022 · event 90073
Official record
FDA enforcement report search

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