RecallHawk
Class II Recall

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

W.Y. Industries, Inc.

Summary

The FDA issued a Class II for WY Duck Sauce, 0.35 oz. (10 g), flexible film packets, 500 packets per case. by W.Y. Industries, Inc.. Reason: Product may contain metal fragments..

Details

Source

Food Recall

External ID

H-1157-2026

Action Date

2026-07-22

Status

Ongoing

Category

food

Product Description

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

Lot/Code Info: UPC codes: 015051010021 Lot code*: 152, after 15:00; 153, any time

Quantity Affected: 1,120 cases of duck sauce packets

Reason for Recall

Product may contain metal fragments.

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2026-06-04

Company

W.Y. Industries, Inc.

North Bergen, NJ

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 39 food recalls issued in the same week, part of 94 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (W.Y. Industries, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does W.Y. Industries, Inc. have FDA actions?

This is the only FDA action we have on record for W.Y. Industries, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1157-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions