Food recall

6174 Industries, LLC recall: SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMENTS NO SOY, NO GLUTEN, NO EGGS, NO...

6174 Industries, LLC, of Huntersville, NC, recalled SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMENTS NO SOY, NO GLUTEN, NO EGGS, NO.... The FDA's reason: “Product was labeled as "gluten free" and it may contain gluten.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on May 5, 2022, and the FDA first listed it in its Enforcement Report of June 15, 2022. 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

Allergen not on the label

Status

Terminated

Closed July 28, 2022

The recall

Company
6174 Industries, LLC (Huntersville, NC)
Reason, in FDA's words
“Product was labeled as "gluten free" and it may contain gluten.”
Where it was sold
Product was shipped to the following states: AR, ID, IL, MI, NH, NV, NY, & TX.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
90073

The product recalled

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

  • F-1154-2022 Class III

    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

    Codes: Lot #392759

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

Get new charts weekly

One email a week with the newest charts and their key numbers. No account needed.

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 June 15, 2022.

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.