RECALL RECORD — CLASS IIIRecall closedF-1154-2022/FDA enforcement

Supple Bears Quercetin Bromelain Gummies + Vitamin C & Zinc 60 Dietary Supplements No Soy, No…

What you need to know

Class III
  • What happened

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

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDAAR, ID, IL, MI +4 moreMore supplements

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Product identification

Source: FDA FOOD

Brand name6174 Industries, LLC
Recalling firm6174 Industries, LLCHuntersville, NC, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #392759
Distribution area
ARIDILMINHNVNYTX

Product was shipped to the following states: AR, ID, IL, MI, NH, NV, NY, & TX.

United States

Quantity affected62cases/50 bottles/60 gummies per bottle
Recall initiationFDA report date: June 15, 2022
FDA recall numberF-1154-2022

Beyond the headline

The recall, in context

6174 Industries, LLC initiated this supplements recall on May 5, 2022. The FDA enforcement report states: Product was labeled as "gluten free" and it may contain gluten. The FDA report lists distribution as: Product was shipped to the following states: AR, ID, IL, MI, NH, NV, NY, & TX.

The FDA enforcement report describes the reason as: Product was labeled as "gluten free" and it may contain gluten.

Supple Bears Quercetin Bromelain Gummies + Vitamin C & Zinc 60 Dietary Supplements No Soy, No… was made or distributed by 6174 Industries, LLC in Huntersville, NC, United States. This page reflects FDA report F-1154-2022, dated June 15, 2022.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared wheat or gluten

Symptoms to watch for

Wheat allergy can cause hives, nausea, cramps, breathing difficulty or anaphylaxis. For celiac disease, even small amounts of gluten can cause intestinal damage.

When symptoms may appear

Allergic reactions can begin within minutes to hours. Celiac-related intestinal effects may be delayed.

Higher-risk groups

People with wheat allergy, celiac disease, non-celiac gluten sensitivity or a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a wheat allergy or must avoid gluten.
  2. 2Seek emergency care for breathing difficulty or other signs of a severe allergic reaction.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Supple Bears Quercetin Bromelain Gummies + Vitamin C & Zinc 60 Dietary Supplements No Soy, No… recall?

6174 Industries, LLC recalled Supple Bears Quercetin Bromelain Gummies + Vitamin C & Zinc 60 Dietary Supplements No Soy, No… in an FDA Class III enforcement action reported as F-1154-2022. Product was labeled as "gluten free" and it may contain gluten.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Do not eat the product if you have a wheat allergy or must avoid gluten. Seek emergency care for breathing difficulty or other signs of a severe allergic reaction. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the 6174 Industries, LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1154-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.