Deep-brand PREMIUM Select Tuvar Lilva Net Wt. 12 oz. (340 g) KEEP F…

CHETAK NEW YORK LLC has recalled Deep-brand PREMIUM Select Tuvar Lilva Net Wt. 12 oz. (340 g) KEEP F…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 17, 2025 and was initiated on September 5, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

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 Deep-brand PREMIUM Select Tuvar Lilva Net Wt. 12 oz. (340 g) KEEP F…, with approximately 3509532 bags affected. The company behind the recall is CHETAK NEW YORK LLC, based in Union, NJ. The FDA describes the product as: “Deep-brand PREMIUM Select Tuvar Lilva Net Wt. 12 oz. (340 g) KEEP FROZEN”

Why was Deep-brand PREMIUM Select Tuvar Lilva Net Wt. 12 oz. (340 g) KEEP F… recalled?

According to the FDA, the stated reason for the recall is: “Product tested positive Salmonella .” In plain terms, this recall relates to Salmonella.

Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.

What should you do?

If you think you may have bought Deep-brand PREMIUM Select Tuvar Lilva Net Wt. 12 oz. (340 g) KEEP F…, compare it against the product description and identifying codes (Lot: 24362, 24363, 24365, 24366, 25003, 25007, 25009, 25010, 25011, 25017, 25034, 25038, 25055, 25065, 25077, 25087, 25088, 25090, 25092, 25106, 25107, 25108,…) before using it.

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 CHETAK NEW YORK LLC or your local health authority.

About this recall

This recall was distributed in NJ. 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.