The Recall Desk
Agency classClass IOur severity:CriticalFDA (Food)·H-0575-2025·Announced 2025-09-03

Sprouted moong recalled after testing positive for Salmonella in packaged product

Deep Sprouted Moong, 16 oz, is recalled after the product tested positive for Salmonella. The FDA classified the action as Class I. 5,616 packets are affected.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The rubric assigns 5 to any FDA Class I recall, and the FDA classified this Salmonella action as Class I.

Plain-English summary

Deep Sprouted Moong, 16 ounces, is being recalled. Affected codes are IN24330, 25072, 25108, 24353, 25171, 24297, 25058, 25078, 24291, 25107, 24354 and 24292. The recall covers 5,616 packets or bags, distributed to California, New Jersey, Illinois, Florida and Texas.

The recall was issued because the product tested positive for Salmonella. The FDA classified the action as Class I, the category the agency uses when there is a reasonable probability that exposure will cause serious health consequences or death.

Anyone holding product matching these codes should not eat it and can return it to the place of purchase.

The recalled product

Product
Deep Sprouted Moong 16 oz
Affected units
5,616

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (11)

  • IN24330
  • 25072
  • 25108
  • 24353
  • 25171
  • 24297
  • 25058
  • 25078
  • 24291
  • 25107
  • 24354 AND 24292

Distribution

Distributed in 5 states:

Part of a larger recall action

This product is one of 2 recalled by CHETAK NEW YORK LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

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