Class IICompletedVoluntary: Firm initiated
Ganesha Enterprises LLC: food recall H-0683-2026
Ganesha Enterprises LLC of Carson City, NV recalled KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, 818812022208, Ganesha Enterprises LLC, 5200… Reason: Undeclared food colorings (Yellow 6, Blue 1, and Yellow 5) and unapproved Acid Red 14. The FDA listed it as Class II in its Enforcement Report dated May 6, 2026; distribution: California, Georgia, Illinois, New York, Tennessee.
Record status as published: Completed. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, 818812022208, Ganesha Enterprises LLC, 5200 Sigstrom Drive, Carson City, Nevada 89706 USA.
- Product quantity
- 347 pieces/ 200 gm pouch
- Reason for recall
- Undeclared food colorings (Yellow 6, Blue 1, and Yellow 5) and unapproved Acid Red 14.
- Codes, lots and dates on the package
- IKS265, 07/2027
- Distribution pattern
- Product was distributed in the following states: CA, GA, IL, NY, and TN.
- Recalling firm
- Ganesha Enterprises LLC, Carson City, NV
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Feb 14, 2026 |
| Classified by the FDA | Apr 30, 2026 |
| Published in the Enforcement Report | May 6, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0683-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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