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RECALL RECORD — CLASS IIIRecall closedF-0350-2023/FDA enforcement
Heidi Remington·Food·Jan 12, 2023

Lemon Almond Blueberry Bread

What you need to know

Class III

  • What happened

    Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products label does not declare Soy Lecithin

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. Tree nuts such as almonds or walnuts were not declared, posing a risk to people with tree-nut allergy.

  • 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 FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameHeidi Remington
Recalling firmHeidi RemingtonTalent, OR, United States
UPC / barcodes
7 21762 76434 3
Lot / date codes
  • Lot code 221227 and Best Used or Freeze By date of 1/6/23. Lot code 230104 and Best Used or Freeze By Date of 1/13/23. Lot code 230109 and Best Used or Freeze By Date of 1/17/23.
Distribution area
IN

distributed in Oregon.

United States

Quantity affected76 packages
Recall initiationFDA report date: February 22, 2023
FDA recall numberF-0350-2023

Beyond the headline

The recall, in context

Heidi Remington initiated this food recall on January 12, 2023. The FDA enforcement report states: Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products label does not declare Soy Lecithin. The FDA report lists distribution as: distributed in Oregon.

The FDA enforcement report describes the reason as: Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products label does not declare Soy Lecithin

Lemon Almond Blueberry Bread was made or distributed by Heidi Remington in Talent, OR, United States. This page reflects FDA report F-0350-2023, dated February 22, 2023.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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 is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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

Undeclared tree nuts

Symptoms to watch for

Hives, swelling, wheezing, digestive symptoms or anaphylaxis can occur in people with a tree-nut 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 tree-nut allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a tree-nut 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 Lemon Almond Blueberry Bread recall?

Heidi Remington recalled Lemon Almond Blueberry Bread in an FDA Class III enforcement action reported as F-0350-2023. Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products label does not declare Soy Lecithin

What are the symptoms of Undeclared tree nuts exposure?

Hives, swelling, wheezing, digestive symptoms or anaphylaxis can occur in people with a tree-nut allergy.

How quickly can Undeclared tree nuts symptoms appear?

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

Who is most at risk from Undeclared tree nuts?

People with a diagnosed tree-nut allergy, especially children and anyone with a history of anaphylaxis.

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 tree-nut 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.

How do I get a refund from Heidi Remington?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0350-2023 and keep the packaging, lot code and proof of purchase if you have them.

Is the Heidi Remington 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-0350-2023. 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

Brand history

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