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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 97300

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 28, 2025
Product types
Food
Classifications
Class I
Statuses
Terminated
Recalling firm wording
CHETAK NEW YORK LLC

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 2

Deep Sprouted Mat 16 oz.

H-0574-2025
Recall number
H-0574-2025
Initiated
June 28, 2025
Classification
Class I
Status
Terminated
Recalling firm
CHETAK NEW YORK LLC
Quantity
5232 PACKET/BAG OF SPROUTED MAT

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product tested positive Salmonella .

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Product tested positive Salmonella .

Code information

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

food · product 2 of 2

Deep Sprouted Moong 16 oz

H-0575-2025
Recall number
H-0575-2025
Initiated
June 28, 2025
Classification
Class I
Status
Terminated
Recalling firm
CHETAK NEW YORK LLC
Quantity
5616 PACKET/BAG OF SPROUTED MOONG

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product tested positive Salmonella .

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Product tested positive Salmonella .

Code information

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