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ACTIVE RECALL — CLASS IIActive recallH-1157-2026/FDA enforcement
W.y. Industries, INC.·Food·Jun 4, 2026

Wy Duck Sauce, 0.35 OZ

What you need to know

Class II

  • What happened

    Product may contain metal fragments.

  • 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.

Active recall · classified by the FDANY, NJ, OH, PAMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameW.y. Industries, INC.
Recalling firmW.y. Industries, INC.North Bergen, NJ, United States
UPC / barcodes
0 15051 01002 1
Lot / date codes
  • UPC codes: 015051010021 Lot code*: 152, after 15:00
  • 153, any time
Distribution area
NYNJOHPA

The adulterated product was distributed to the following states : NY, NJ, OH, PA

United States

Quantity affected1, 120 cases of duck sauce packets
Recall initiationFDA report date: July 22, 2026
FDA recall numberH-1157-2026

Beyond the headline

The recall, in context

W.y. Industries, INC. initiated this food recall on June 4, 2026. The FDA enforcement report states: Product may contain metal fragments. The FDA report lists distribution as: The adulterated product was distributed to the following states : NY, NJ, OH, PA.

The FDA enforcement report describes the reason as: Product may contain metal fragments.

Wy Duck Sauce, 0.35 OZ was made or distributed by W.y. Industries, INC. in North Bergen, NJ, United States. This page reflects FDA report H-1157-2026, dated July 22, 2026.

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 Wy Duck Sauce, 0.35 OZ recall?

W.y. Industries, INC. recalled Wy Duck Sauce, 0.35 OZ in an FDA Class II enforcement action reported as H-1157-2026. Product may contain metal fragments.

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.

Is the W.y. Industries, INC. recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-1157-2026. 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.