SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMENTS NO SOY, NO GLUTEN, NO EGGS, NO DIARY,
Summary
The FDA issued a Class III for SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMEN by 6174 Industries, LLC. Reason: Product was labeled as "gluten free" and it may contain gluten..
Details
Source
Food Recall
External ID
F-1154-2022
Action Date
2022-06-15
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Lot #392759
Quantity Affected: 62cases/50 bottles/60 gummies per bottle
Reason for Recall
Product was labeled as "gluten free" and it may contain gluten.
Distribution
Product was shipped to the following states: AR, ID, IL, MI, NH, NV, NY, & TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-05
Company
Huntersville, NC
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 197 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (6174 Industries, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does 6174 Industries, LLC have FDA actions?
This is the only FDA action we have on record for 6174 Industries, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1154-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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