Reshmi's Group Inc. Recall: Undeclared wheat. Sooji Coarse is recalled because product contains Semolina but wheat is not declared on label.
United States
TerminatedClass II
- Company
- Reshmi's Group Inc.
- Product
- Sooji Coarse, Siva's brand, packaged in 2 lbs. and 4 lbs pol…
- Recall date
- July 10, 2017
- Terminated
- June 18, 2018
- Source
- FDA
Reason for recall
Undeclared wheat. Sooji Coarse is recalled because product contains Semolina but wheat is not declared on label.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Sooji Coarse, Siva's brand, packaged in 2 lbs. and 4 lbs poly bags. UPC for 2 lbs. package is 8 46499 00316 1 UPC for 4 lbs. package is 8 46499 00186 5. The label is read in parts: "***Ingredients: Sooji Coarse***Siva's***LOW FAT, GOOD SOURCE OF IRON, SOURCE OF FIBER, CHOLESTEROL FREE***Imported & Marketed by Reshmi's Group, Inc 6845 S. 220th ST KENT, WA 98032***". | Not published in this source record | 30 cases (20/2 lbs. package per case) AND 32 cases (10/4 lbs. packages per case) | none |
Distribution
- distributed in ID
- OR and WA.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0305-2017
- Event ID
- 77714
- Status
- Terminated
- Classification
- Class II
- Company
- Reshmi's Group Inc.
- Product description
- Sooji Coarse, Siva's brand, packaged in 2 lbs. and 4 lbs poly bags. UPC for 2 lbs. package is 8 46499 00316 1 UPC for 4 lbs. package is 8 46499 00186 5. The label is read in parts: "***Ingredients: Sooji Coarse***Siva's***LOW FAT, GOOD SOURCE OF IRON, SOURCE OF FIBER, CHOLESTEROL FREE***Imported & Marketed by Reshmi's Group, Inc 6845 S. 220th ST KENT, WA 98032***".
- Quantity
- 30 cases (20/2 lbs. package per case) AND 32 cases (10/4 lbs. packages per case)
- Reason
- Undeclared wheat. Sooji Coarse is recalled because product contains Semolina but wheat is not declared on label.
- Recall initiation date
- July 10, 2017
- Report date
- July 26, 2017
- Classification date
- Not published in this source record
- Termination date
- June 18, 2018
- Distribution pattern
- distributed in ID, OR and WA.
- UPC, lot, and code information
- none
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Reshmi's Group Inc.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Idaho | 1 |
| Oregon | 1 |
| Washington | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
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