Ganesha KLG Kesar Mukhwas Recall: Undeclared Food Colorings Hazard
Ganesha Enterprises recalls KLG Kesar Mukhwas due to undeclared food colorings (Yellow 6, Blue 1, Yellow 5) and unapproved Acid Red 14. This may pose health risks. Check product code 818812022208 for affected items.
Recall notice
Undeclared food colorings (Yellow 6, Blue 1, and Yellow 5) and unapproved Acid Red 14.
Contact the company
What happened, in plain English
Ganesha Enterprises is recalling KLG Kesar Mukhwas products because they contain undeclared food colorings and unapproved dyes. This could lead to health issues if consumed. Consumers should check the product code to see if they have affected items. Read more at govinfonow.com/recall/6738-ganesha-klg-kesar-mukhwas-recall-undeclared-food-colorings-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/6738-ganesha-klg-kesar-mukhwas-recall-undeclared-food-colorings-hazard · Updated August 17, 2026 · Official notice: FDA #H-0683-2026
Cite this page
“Ganesha KLG Kesar Mukhwas Recall: Undeclared Food Colorings Hazard.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6738-ganesha-klg-kesar-mukhwas-recall-undeclared-food-colorings-hazard. Based on FDA recall #H-0683-2026.
Why it’s dangerous
The product contains undeclared food colorings (Yellow 6, Blue 1, Yellow 5) and unapproved Acid Red 14. These dyes are not approved for use in food products and could cause health issues if consumed.
Who’s affected
Anyone who purchased KLG Kesar Mukhwas with the product code 818812022208 from Ganesha Enterprises. Children and individuals with sensitivities to food dyes may be at higher risk.
How to tell if you have this one
Check for the product code 818812022208 on the packaging. The product is a perishable, flexible plastic container with a 200 gm size.
- Brand
Ganesha Enterprises- Category
Food
What to do — step by step
Check Product Code
Look for the product code 818812022208 on the packaging to confirm if you have an affected item.
Where it went and when
Where it was distributed
Distributed in 5 states.
FDA distribution: “Product was distributed in the following states: CA, GA, IL, NY, and TN.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Georgia, Illinois, New York, Tennessee.
Recall timeline
FDA published this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #H-0683-2026 (February 14, 2026)
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.