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RECALL RECORD — CLASS IIRecall closedF-1967-2012/FDA enforcement
Breadfarm·Food·Jun 26, 2012

Wheat Crackers, Packaged in Cellophane Sleeve Wrap, 6.4 OZ Each

What you need to know

Class II

  • What happened

    The wheat germ used by the firm to make their products was recalled by the wheat germ manufacturer because it was potentially contaminated with metal fragments approximately…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Metal fragments can cause cuts, choking or internal injury if swallowed.

  • 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 nameBreadfarm
Recalling firmBreadfarmBow, WA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • "122", "130", "137", "148", "165". These are the julian dates that the dough was made, baked and packaged.
Distribution area
IN

Distributed to retailers and direct accounts in Washington State.

United States

Quantity affected163, 6.4oz packages
Recall initiationFDA report date: August 29, 2012
FDA recall numberF-1967-2012

Beyond the headline

The recall, in context

Breadfarm initiated this food recall on June 26, 2012. The FDA enforcement report states: The wheat germ used by the firm to make their products was recalled by the wheat germ manufacturer because it was potentially contaminated with metal fragments approximately 05.mm in diameter and 3-15 mm in length. The contamination occurred at the raw ingredient manufacturer. The FDA report lists distribution as: Distributed to retailers and direct accounts in Washington State.

The FDA enforcement report describes the reason as: The wheat germ used by the firm to make their products was recalled by the wheat germ manufacturer because it was potentially contaminated with metal fragments approximately 05.mm in diameter and 3-15 mm in length. The contamination occurred at the raw ingredient manufacturer.

Wheat Crackers, Packaged in Cellophane Sleeve Wrap, 6.4 OZ Each was made or distributed by Breadfarm in Bow, WA, United States. This page reflects FDA report F-1967-2012, dated August 29, 2012.

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, metal fragments can cause cuts, choking or internal injury if swallowed.

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

Metal contamination

Possible health effects

Metal fragments can cause cuts, choking or internal injury. Do not inspect or taste a suspect product.

Higher-risk groups

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk.

What to do now

  1. 1Stop eating or using the product; do not try to find the fragment by tasting or chewing.
  2. 2Seek medical care if anyone has swallowed metal or has severe throat, chest or abdominal pain.
  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 Wheat Crackers, Packaged in Cellophane Sleeve Wrap, 6.4 OZ Each recall?

Breadfarm recalled Wheat Crackers, Packaged in Cellophane Sleeve Wrap, 6.4 OZ Each in an FDA Class II enforcement action reported as F-1967-2012. The wheat germ used by the firm to make their products was recalled by the wheat germ manufacturer because it was potentially contaminated with metal fragments approximately…

What injuries or health effects are linked to metal contamination?

Metal fragments can cause cuts, choking or internal injury. Do not inspect or taste a suspect product.

Who is most at risk from Metal contamination?

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk.

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 eating or using the product; do not try to find the fragment by tasting or chewing. Seek medical care if anyone has swallowed metal or has severe throat, chest or abdominal pain. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Breadfarm?

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-1967-2012 and keep the packaging, lot code and proof of purchase if you have them.

Is the Breadfarm 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-1967-2012. 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.