Recall record at a glance
| Official record | F-0305-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Reshmi's Group Inc. |
| Report date | Jul 26, 2017 |
| Recall initiation date | Jul 10, 2017 |
| Quantity | 30 cases (20/2 lbs. package per case) AND 32 cases (10/4 lbs. packages per case) |
| Location | Tukwila, WA, United States |
Official 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***".
Why the product was recalled
Undeclared wheat. Sooji Coarse is recalled because product contains Semolina but wheat is not declared on label.
Distribution information
distributed in ID, OR and WA.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.