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Lower risk Food recall · FDA · Published June 4, 2026

WY Duck Sauce Recall: Metal Fragments in Packets

WY Duck Sauce flexible film packets may contain metal fragments. Recalled lots 152 (after 15:00) and 153 (any time) with UPC 015051010021. Consumers should check their packaging.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-1157-2026FoodW.Y. Industries ›
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Contact the company

Recalling firmW.Y. Industries, Inc.2500 Secaucus Rd · North Bergen, NJ 07047-1553
✎ GovInfoNow plain-language explainer

W.Y. Industries is recalling 500-packet cases of WY Duck Sauce due to potential metal fragments in the sauce. This could cause injury if metal pieces are ingested. Consumers should check their packaging for the lot code and UPC. Read more at govinfonow.com/recall/6192-wy-duck-sauce-recall-metal-fragments-in-packets.

Source Summary by GovInfoNow · govinfonow.com/recall/6192-wy-duck-sauce-recall-metal-fragments-in-packets · Updated August 7, 2026 · Official notice: FDA #H-1157-2026

Cite this page

“WY Duck Sauce Recall: Metal Fragments in Packets.” GovInfoNow, updated August 7, 2026. https://govinfonow.com/recall/6192-wy-duck-sauce-recall-metal-fragments-in-packets. Based on FDA recall #H-1157-2026.

The FDA announced on June 4, 2026, that W.Y. Industries, Inc. is recalling WY Duck Sauce flexible film packets due to the potential presence of metal fragments. The voluntary Class II recall affects 1,120 cases distributed to New York, New Jersey, Ohio, and Pennsylvania.

How to tell if you have it

  • Brand: W.Y. Industries
  • Product: WY Duck Sauce, 0.35 oz. (10 g), flexible film packets
  • UPC: 00015051010021
  • Lot codes: 152 (after 15:00) and 153 (any time)
  • Quantity: 500 packets per case

The hazard

The product may contain metal fragments, according to the FDA. The agency classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include Ukrop's Bread Pudding with Vanilla Sauce Recall (2026-07-30) and Woodstock Organic Edamame Recall (2026-04-21). Ajinomoto Vegetable Gyoza Dumplings Recall involving foreign glass objects was reported on 2026-03-03.

How to tell if you have this one

Check the packaging for the lot code (152 after 15:00 or 153 any time) and UPC code 015051010021. The product is sold in 500-packet cases.

  • Brand
    W.Y. Industries
  • Product
    WY Duck Sauce, 0.35 oz. (10 g), flexible film packets, 500 packets per case
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Packaging

    Look for the lot code on the packaging: 152 after 15:00 or 153 any time, with UPC 015051010021.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “The adulterated product was distributed to the following states : NY, NJ, OH, PA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New Jersey, New York, Ohio, Pennsylvania.

Recall timeline

FDA published this recall 48 days after the firm started it.

1. Firm started the recall: Jun 4, 202612. FDA classified it Class II: Jul 14, 202623. Published in FDA’s Enforcement Report: Jul 22, 202632026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-1157-2026 (June 4, 2026)
  • Plain-language summary written by qwen3:4b on August 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA