CLASS I Food recall · Reported 5 Jun 2019 · FDA Enforcement Report

Laxmi Dried Apricot Plastic recalled by House of Spices India

House of Spices India is recalling Laxmi Dried Apricot Plastic, distributed nationwide in the US. The recall was initiated on 17 May 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll Lot Codes
Quantity recalled22680 Pouches

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-1443-2019
FDA event ID
82902
Recalling firm
House of Spices India, New Hyde Park, NY
Brand
Laxmi
Classification
Class I
Status
Terminated
Recall initiated
17 May 2019
FDA classified
8 Jun 2019
Reported
5 Jun 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sulfites
Product category
Fish

Timeline

17 May 2019Recall initiated by company
5 Jun 2019Published in enforcement report+19 days
8 Jun 2019Classified by FDA+3 days

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

Reason for recall

Product contains elevated levels of undeclared Sulfites

Product as listed by the FDA

Laxmi Brand Dried Apricot 7 oz (200g) Plastic Pouch UPC Code: 2324617054

Where it was distributed

Nationwide and two foreign consignees

Nationwide

Questions about this recall

Why was it recalled?

Product contains elevated levels of undeclared Sulfites

Which lots are affected?

All Lot Codes

Where was it sold?

Nationwide and two foreign consignees

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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