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RECALL RECORD — CLASS IRecall closedF-1038-2015/FDA enforcement
Regional Access INC·Food·Dec 26, 2014

Cumin Seed, Ground, Packed as NET WT 1 lb, Reorder: #Hs300, and NET WT 5 lb, Reorder: #Hs310

What you need to know

Class I

  • What happened

    Cumin may contain undeclared peanut protein.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDANYMore food

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Product identification

Source: FDA FOOD

Brand nameRegional Access INC
Recalling firmRegional Access INCIthaca, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Packed on: 7/29/2014
Distribution area
NY

NY

United States

Quantity affected50 lbs (repacked into 20/1 lb and 6/5 lb bags)
Recall initiationFDA report date: February 18, 2015
FDA recall numberF-1038-2015

Beyond the headline

The recall, in context

Regional Access INC initiated this food recall on December 26, 2014. The FDA enforcement report states: Cumin may contain undeclared peanut protein. The FDA report lists distribution as: NY.

The FDA enforcement report describes the reason as: Cumin may contain undeclared peanut protein.

Cumin Seed, Ground, Packed as NET WT 1 lb, Reorder: #Hs300, and NET WT 5 lb, Reorder: #Hs310 was made or distributed by Regional Access INC in Ithaca, NY, United States. This page reflects FDA report F-1038-2015, dated February 18, 2015.

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, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

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 lot and date codes 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

Undeclared peanut

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a peanut allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed peanut allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a peanut allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 Cumin Seed, Ground, Packed as NET WT 1 lb, Reorder: #Hs300, and NET WT 5 lb, Reorder: #Hs310 recall?

Regional Access INC recalled Cumin Seed, Ground, Packed as NET WT 1 lb, Reorder: #Hs300, and NET WT 5 lb, Reorder: #Hs310 in an FDA Class I enforcement action reported as F-1038-2015. Cumin may contain undeclared peanut protein.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a peanut allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Regional Access 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-1038-2015. 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

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