Chetak New York LLC food recall: Deep Sprouted Mat 16 oz
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97300
- Recall initiated
- Jun 28, 2025
- Classified by FDA
- Sep 8, 2025
- Posted in Enforcement Report
- Sep 3, 2025
- Terminated
- Oct 28, 2025
- Recalling firm
- CHETAK NEW YORK LLC
- Firm location
- Union, NJ, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 2
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Product tested positive Salmonella .
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Jun 28, 2025. FDA classified it 72 days later, on Sep 8, 2025. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: Th recalled product was distributed to the following States: CA, NJ, IL, FL, TX CHETAK NEW YORK LLC has 4 recalls in our records.
Recalled products (2)
H-0574-2025 Class I Terminated
Deep Sprouted Mat 16 oz.
Codes / lots: IN24330,25072,25108,24353,25171,24297,25058,25078,24291,25107,24354 AND 24292
Quantity: 5232 PACKET/BAG OF SPROUTED MAT
H-0575-2025 Class I Terminated
Deep Sprouted Moong 16 oz
Codes / lots: IN24330,25072,25108,24353,25171,24297,25058,25078,24291,25107,24354 AND 24292
Quantity: 5616 PACKET/BAG OF SPROUTED MOONG
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 97300
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.