KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm

Ganesha Enterprises LLC has recalled KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 6, 2026 and was initiated on February 14, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, with approximately 347 pieces/ 200 gm pouch affected. The company behind the recall is Ganesha Enterprises LLC, based in Carson City, NV. The FDA describes the product as: “KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, 818812022208, Ganesha Enterprises LLC, 5200 Sigstrom Drive, Carson City, Nevada 89706 USA.”

Why was KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm recalled?

According to the FDA, the stated reason for the recall is: “Undeclared food colorings (Yellow 6, Blue 1, and Yellow 5) and unapproved Acid Red 14.” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, compare it against the product description and identifying codes (IKS265, 07/2027) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Ganesha Enterprises LLC or your local health authority.

About this recall

This recall was distributed in NV. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.