CLASS II Food recall · Reported 27 Sep 2017 · FDA Enforcement Report

Laxmi Rusks recalled by House of Spices India

House of Spices India is recalling Laxmi Rusks, distributed in California, Georgia, Maryland, New York, Texas. The recall was initiated on 24 Aug 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch numbers L102516, L011217, L031817, L041417, L041517, L041617, and L060717
Quantity recalledunknown

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-3571-2017
FDA event ID
78018
Recalling firm
House of Spices India, Flushing, NY
Classification
Class II
Status
Terminated
Recall initiated
24 Aug 2017
FDA classified
20 Sep 2017
Reported
27 Sep 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Soy
Product category
Fish

Timeline

24 Aug 2017Recall initiated by company
20 Sep 2017Classified by FDA+27 days
27 Sep 2017Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product may contain undeclared soy.

Product as listed by the FDA

Laxmi Rusks, 10.58 OZ (300 gram) bags; UPC Code: 7 23246 26482 0

Where it was distributed

TX, CA, GA, MD, NY

CaliforniaGeorgiaMarylandNew YorkTexas

Questions about this recall

Why was it recalled?

Product may contain undeclared soy.

Which lots are affected?

Batch numbers L102516, L011217, L031817, L041417, L041517, L041617, and L060717

Where was it sold?

TX, CA, GA, MD, NY

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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