RECALL RECORD — CLASS IIRecall closedF-0301-2025/FDA enforcement

Baguette, Artisan Multigrain

What you need to know

Class II
  • What happened

    Possible contamination by a foreign object (metal) in sub-ingredient in dinner roll product

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameStuyvers Bread (Premium Brand Bakery Division)
Recalling firmStuyvers Bread (Premium Brand Bakery Division)Langley, Canada
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • SKU#24313
Distribution area
IN

product was distributed to two consignees in 3 different states (California, Connecticut, Washington)

United States

Quantity affected108 cases
Recall initiationFDA report date: December 25, 2024
FDA recall numberF-0301-2025

Beyond the headline

The recall, in context

Stuyvers Bread (Premium Brand Bakery Division) initiated this food recall on November 13, 2024. The FDA enforcement report states: Possible contamination by a foreign object (metal) in sub-ingredient in dinner roll product. The FDA report lists distribution as: product was distributed to two consignees in 3 different states (California, Connecticut, Washington).

The FDA enforcement report describes the reason as: Possible contamination by a foreign object (metal) in sub-ingredient in dinner roll product

Baguette, Artisan Multigrain was made or distributed by Stuyvers Bread (Premium Brand Bakery Division) in Langley, Canada. This page reflects FDA report F-0301-2025, dated December 25, 2024.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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

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 Baguette, Artisan Multigrain recall?

Stuyvers Bread (Premium Brand Bakery Division) recalled Baguette, Artisan Multigrain in an FDA Class II enforcement action reported as F-0301-2025. Possible contamination by a foreign object (metal) in sub-ingredient in dinner roll product

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

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

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.

How do I get a refund from Stuyvers Bread (Premium Brand Bakery Division)?

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-0301-2025 and keep the packaging, lot code and proof of purchase if you have them.

Is the Stuyvers Bread (Premium Brand Bakery Division) 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-0301-2025. 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.