Class II Recall

Park St. Deli Macaroni & Cheese, NET WT 20 OZ (1 LB 4 OZ) 567g, product packed in plastic tub and placed into paperboard

Summary

The FDA issued a Class II for Park St. Deli Macaroni & Cheese, NET WT 20 OZ (1 LB 4 OZ) 567g, product packed i by BEF Foods, Inc. Reason: Undeclared allergen (soy lecithin)..

Details

Source

Food Recall

External ID

H-0940-2026

Action Date

2026-06-17

Status

Ongoing

Product Description

Park St. Deli Macaroni & Cheese, NET WT 20 OZ (1 LB 4 OZ) 567g, product packed in plastic tub and placed into paperboard sleeve. 9/20 oz packages per case.

Lot/Code Info: SUL4839705; SUL4839706; SUL4853771; SUL4853772; SUL4854698; SUL4854700; SUL4854701; SUL4855698; SUL4855699; SUL4855700; SUL4857735; SUL4857736; SUL4857737; SUL4857784; SUL4857785; SUL4866750; SUL4866751; SUL4866752; SUL4866781; SUL4866782; SUL4866783; SUL4866784; SUL4872813; SUL4872814; SUL4872815; SUL4873787; SUL4873788; SUL4886739; SUL4886740; SUL4887698; SUL4887699

Quantity Affected: 58,405 cases (9-20 oz packages/case)

Reason for Recall

Undeclared allergen (soy lecithin).

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-23

Company

BEF Foods, Inc

Sulphur Springs, TX

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 191 food recalls issued in the same week, part of 204 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 (BEF Foods, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does BEF Foods, Inc have FDA actions?

This is the only FDA action we have on record for BEF Foods, Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0940-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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