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Stop using now Food recall · FDA · Published July 10, 2017

Siva's Sooji Coarse Recall: Undeclared Wheat Hazard

Siva's brand Sooji Coarse is recalled due to undeclared wheat. Check your UPCs and consult the remedy for affected packages.

🇺🇸 FDA recall #F-0305-2017FoodSiva's ›
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Contact the company

Recalling firmReshmi's Group Inc.1120 Andover Park E · Tukwila, WA 98188-3903
✎ GovInfoNow plain-language explainer

What happened, in plain English

Reshmi's Group Inc. is recalling Siva's brand Sooji Coarse because it contains semolina, which includes wheat, but the label does not declare this allergen. This poses a risk to individuals with wheat allergies or celiac disease who may unknowingly consume the product. The recall covers specific packages distributed in Idaho, Oregon, and Washington. Read more at govinfonow.com/recall/20668-siva-s-sooji-coarse-recall-undeclared-wheat-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/20668-siva-s-sooji-coarse-recall-undeclared-wheat-hazard · Updated October 11, 2026 · FDA enforcement record: FDA #F-0305-2017

Cite this page

“Siva's Sooji Coarse Recall: Undeclared Wheat Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20668-siva-s-sooji-coarse-recall-undeclared-wheat-hazard. Based on FDA recall #F-0305-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0305-2017%22&limit=1).

Why it’s dangerous

The product contains semolina, a form of wheat, which is not listed on the ingredients label. For people with wheat allergies or celiac disease, consuming undeclared wheat can trigger serious allergic reactions or other health complications.

Who’s affected

Consumers who purchased Siva's brand Sooji Coarse in 2 lbs. or 4 lbs. poly bags from stores in Idaho, Oregon, or Washington. Individuals with wheat allergies or celiac disease are at the highest risk of an allergic reaction.

How to tell if you have this one

Check if you have Siva's brand Sooji Coarse packaged in 2 lbs. or 4 lbs. poly bags. Verify the UPC code: 8 46499 00316 1 for the 2 lbs. package or 8 46499 00186 5 for the 4 lbs. package. The label will state "Imported & Marketed by Reshmi's Group, Inc" with an address in Kent, WA.

  • Brand
    Siva's
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Sooji Coarse if you have any of the recalled UPC codes or packages from the affected distribution areas.

  2. Check your package details

    Look for the specific UPCs (8 46499 00316 1 or 8 46499 00186 5) and the "Siva's" brand name on the packaging.

  3. Contact the manufacturer

    Reach out to Reshmi's Group Inc. for further instructions or refunds, as specific remedy details are not provided in this record.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: yesIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “distributed in ID, OR and WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Idaho, Oregon, Washington.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Jul 10, 201712. FDA classified it Class II: Jul 19, 201723. Published in FDA’s Enforcement Report: Jul 26, 201734. FDA terminated the recall: Jun 18, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0305-2017 (July 10, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0305-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA