FDAClass II · Food · Recall H-1157-2026 · Recalled July 22, 2026

WY Duck Sauce recall — W.Y. Industries, Inc.

Agency report date: July 22, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: WY Duck Sauce
Company / brand: W.Y. Industries
Lot / serial / date codes: UPC codes: 015051010021 Lot code*: 152, after 15:00; 153, any time
Distribution: The adulterated product was distributed to the following states : NY, NJ, OH, PA

Agency product description and boundaries

WY Duck Sauce, 0.35 oz. (10 g), flexible film packets, 500 packets per case.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Product may contain metal fragments.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: WY Duck Sauce

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1157-2026
Brand: W.Y. Industries
Classification: Class II
Units affected: 1,120 cases of duck sauce packets
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

WY Duck Sauce

Companies & origin

Recalling firm location: North Bergen, NJ, United States
Firm address: 2500 Secaucus Rd, 07047-1553

Identifying details (verbatim from the notice)

Product codes / lots: UPC codes: 015051010021 Lot code*: 152, after 15:00; 153, any time
Distribution: The adulterated product was distributed to the following states : NY, NJ, OH, PA
Firm notified the public via: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID: 99238
Recall initiated: June 4, 2026
FDA classified: July 14, 2026
FDA report date: July 22, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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