RECALL RECORD — CLASS IRecall closedF-0804-2013/FDA enforcement

Sukhi's Gourmet Indian Food

What you need to know

Class I
  • What happened

    A consumer complaint determined that some boxes of Red Curry and Vegetables were inadvertently packaged with Yellow Curry with Shrimp.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAIN, CA, TX, MN +3 moreMore food

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Match before you discard

Product identification

Source: FDA FOOD

Brand nameJagpreet Enterprises INC.
Recalling firmJagpreet Enterprises INC.Hayward, CA, United States
UPC / barcodes
7 76226 02901 6
Lot / date codes
  • Lot code: 3390113612
  • Use by Date: 05/14/2013
  • UPC 7-76226-02901-6
Distribution area
INCATXMNGACOWA

IN, CA, TX, MN, GA, CO, WA

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: December 12, 2012
FDA recall numberF-0804-2013

Beyond the headline

The recall, in context

Jagpreet Enterprises INC. initiated this food recall on November 20, 2012. The FDA enforcement report states: A consumer complaint determined that some boxes of Red Curry and Vegetables were inadvertently packaged with Yellow Curry with Shrimp. The FDA report lists distribution as: IN, CA, TX, MN, GA, CO, WA.

The FDA enforcement report describes the reason as: A consumer complaint determined that some boxes of Red Curry and Vegetables were inadvertently packaged with Yellow Curry with Shrimp.

Sukhi's Gourmet Indian Food was made or distributed by Jagpreet Enterprises INC. in Hayward, CA, United States. This page reflects FDA report F-0804-2013, dated December 12, 2012.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Sukhi's Gourmet Indian Food recall?

Jagpreet Enterprises INC. recalled Sukhi's Gourmet Indian Food in an FDA Class I enforcement action reported as F-0804-2013. A consumer complaint determined that some boxes of Red Curry and Vegetables were inadvertently packaged with Yellow Curry with Shrimp.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Jagpreet Enterprises INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0804-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Related alerts

Recent Other safety concern recalls

All alerts

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.