Class ITerminatedVoluntary: Firm initiated
CHETAK NEW YORK LLC: food recall H-0574-2025
CHETAK NEW YORK LLC of Union, NJ recalled Deep Sprouted Mat 16 oz. Reason: Product tested positive Salmonella . The FDA listed it as Class I in its Enforcement Report dated Sep 3, 2025; distribution: California, Florida, Illinois, New Jersey, Texas.
Record status as published: Terminated (terminated Oct 28, 2025). 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
- Deep Sprouted Mat 16 oz.
- Product quantity
- 5232 PACKET/BAG OF SPROUTED MAT
- Reason for recall
- Product tested positive Salmonella .
- Codes, lots and dates on the package
- IN24330,25072,25108,24353,25171,24297,25058,25078,24291,25107,24354 AND 24292
- Distribution pattern
- Th recalled product was distributed to the following States: CA, NJ, IL, FL, TX
- Recalling firm
- CHETAK NEW YORK LLC, Union, NJ
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jun 28, 2025 |
| Classified by the FDA | Sep 8, 2025 |
| Published in the Enforcement Report | Sep 3, 2025 |
| Terminated | Oct 28, 2025 |
Other products in the same recall event
The FDA groups related products under one recall event (event 97300).
- H-0575-2025 — Deep Sprouted Moong 16 oz
Other recalls by CHETAK NEW YORK LLC
- H-0301-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0300-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0299-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0298-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0297-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0296-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0295-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0294-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0293-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
- H-0292-2026 · Dec 17, 2025 · Class I — Product tested positive Salmonella .
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OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0574-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.