Summary
The FDA issued a Class I for Deep Sprouted Moong 16 oz by CHETAK NEW YORK LLC. Reason: Product tested positive Salmonella ..
Details
Source
Food Recall
External ID
H-0575-2025
Action Date
2025-09-03
Status
Terminated
Category
food
Product Description
Deep Sprouted Moong 16 oz
Lot/Code Info: IN24330,25072,25108,24353,25171,24297,25058,25078,24291,25107,24354 AND 24292
Quantity Affected: 5616 PACKET/BAG OF SPROUTED MOONG
Reason for Recall
Product tested positive Salmonella .
Distribution
Th recalled product was distributed to the following States: CA, NJ, IL, FL, TX
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-28
Company
Union, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 43 food recalls issued in the same week, part of 204 food-related FDA actions this month.
CHETAK NEW YORK LLC has 54 FDA actions in our database, including 54 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (CHETAK NEW YORK LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does CHETAK NEW YORK LLC have FDA actions?
CHETAK NEW YORK LLC has 54 FDA actions in our database, including 54 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0575-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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