House of Spices Laxmi Rusks Recall: Undeclared Soy in Product
House of Spices India, Inc. recalls Laxmi Rusks bags due to potential undeclared soy content. Affected products include specific UPC codes and batch numbers. Consumers should check their purchases and contact the company for details.
Lower-risk recall
Product may contain undeclared soy.
Contact the company
What happened, in plain English
House of Spices India, Inc. is recalling Laxmi Rusks bags that may contain undeclared soy. This recall affects consumers with allergies to soy, as the product is not labeled for soy content. Read more at govinfonow.com/recall/20478-house-of-spices-laxmi-rusks-recall-undeclared-soy-in-product.
Source Summary by GovInfoNow · govinfonow.com/recall/20478-house-of-spices-laxmi-rusks-recall-undeclared-soy-in-product · Updated October 7, 2026 · FDA enforcement record: FDA #F-3571-2017
Cite this page
“House of Spices Laxmi Rusks Recall: Undeclared Soy in Product.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20478-house-of-spices-laxmi-rusks-recall-undeclared-soy-in-product. Based on FDA recall #F-3571-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3571-2017%22&limit=1).
Why it’s dangerous
The product may contain soy without being labeled, which poses a risk for individuals with soy allergies. This is a food safety issue that could lead to allergic reactions if the product is consumed.
Who’s affected
People with soy allergies are most at risk from these Laxmi Rusks bags. The recall applies to specific batch numbers and UPC codes sold in the U.S.
How to tell if you have this one
Check for the UPC code 7 23246 26482 0 on the bag. Affected batches include L102516, L011217, L031817, L041417, L041517, L041617, and L060717.
- Brand
House of Spices- Product
Laxmi Rusks, 10.58 OZ (300 gram) bags; UPC Code: 7 23246 26482 0- Category
Food
What to do — step by step
Check Product Details
Look for the UPC code 7 23246 26482 0 and batch numbers listed in the recall.
Where it went and when
Where it was distributed
Distributed in 5 states.
FDA distribution: “TX, CA, GA, MD, NY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Georgia, Maryland, New York, Texas.
Recall timeline
FDA terminated this recall 23 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- 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-3571-2017 (August 24, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3571-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.