RECALL RECORD — CLASS IIRecall closedF-0741-2016/FDA enforcement

Cornstach Packaged in a 50lb

What you need to know

Class II
  • What happened

    Food grade Cornstarch may contain metal fragments >1 mm in width and up to 50 mm in length.

  • 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 FDADistribution not listedMore food

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Product identification

Source: FDA FOOD

Brand nameIngredion Incorporated
Recalling firmIngredion IncorporatedWestchester, IL, United States
UPC / barcodes
2 60535 36510 2
Lot / date codes
  • batch numbers: 2605354100, 2605361100, 2605361101, 2605362101, 260535365102, 2606012101, 2606013101.
Distribution area

The product was shipped to 2 U.S. firm ins: Cereal Ingredients Inc. 4720 S. 13th St, Leavenworth Kansas, 606048 and Rohtstein Corp, Walnut Hill Station, 70 Olympia Ave, Woburn, Mashachusetts. The product was also distributed to foreign firms, please see attached documents.

United States

Quantity affected1, 402, 243 lbs. of product. product was shipped in 50 lb. bags.
Recall initiationFDA report date: March 16, 2016
FDA recall numberF-0741-2016

Beyond the headline

The recall, in context

Ingredion Incorporated initiated this food recall on February 9, 2016. The FDA enforcement report states: Food grade Cornstarch may contain metal fragments >1 mm in width and up to 50 mm in length. The FDA report lists distribution as: The product was shipped to 2 U.S. firm ins: Cereal Ingredients Inc. 4720 S. 13th St, Leavenworth Kansas, 606048 and Rohtstein Corp, Walnut Hill Station, 70 Olympia Ave, Woburn, Mashachusetts. The product was also distributed to foreign firms, please see attached documents.

The FDA enforcement report describes the reason as: Food grade Cornstarch may contain metal fragments >1 mm in width and up to 50 mm in length.

Cornstach Packaged in a 50lb was made or distributed by Ingredion Incorporated in Westchester, IL, United States. This page reflects FDA report F-0741-2016, dated March 16, 2016.

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 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

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 Cornstach Packaged in a 50lb recall?

Ingredion Incorporated recalled Cornstach Packaged in a 50lb in an FDA Class II enforcement action reported as F-0741-2016. Food grade Cornstarch may contain metal fragments >1 mm in width and up to 50 mm in length.

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 Ingredion Incorporated?

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-0741-2016 and keep the packaging, lot code and proof of purchase if you have them.

Is the Ingredion Incorporated 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-0741-2016. 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.