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Lower risk Food recall · FDA · Published March 23, 2026

BEF Foods Park St. Deli Macaroni & Cheese Recall: Undeclared Soy Lecithin Allergen

BEF Foods recalls Park St. Deli Macaroni & Cheese (20 oz) due to undeclared soy lecithin allergen. Consumers should check product codes and contact BEF Foods for details.

🇺🇸 FDA recall #H-0940-2026FoodBEF Foods ›
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Contact the company

Recalling firmBEF Foods, Inc1109 Industrial Dr E · Sulphur Springs, TX 75482-3326
✎ GovInfoNow plain-language explainer

BEF Foods is recalling Park St. Deli Macaroni & Cheese (20 oz) because it contains soy lecithin, an allergen not declared on the label. This poses a risk for people with soy allergies. The recall affects specific product codes sold in certain packaging. Read more at govinfonow.com/recall/6644-bef-foods-park-st-deli-macaroni-cheese-recall-undeclared-soy.

Source Summary by GovInfoNow · govinfonow.com/recall/6644-bef-foods-park-st-deli-macaroni-cheese-recall-undeclared-soy · Updated August 10, 2026 · Official notice: FDA #H-0940-2026

Cite this page

“BEF Foods Park St. Deli Macaroni & Cheese Recall: Undeclared Soy Lecithin Allergen.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/6644-bef-foods-park-st-deli-macaroni-cheese-recall-undeclared-soy. Based on FDA recall #H-0940-2026.

The FDA announced on March 23, 2026, that BEF Foods, Inc. is recalling Park St. Deli Macaroni & Cheese due to an undeclared soy lecithin allergen. Consumers should check lot codes and contact the company for a refund.

How to tell if you have it

  • Brand: BEF Foods
  • Product: Park St. Deli Macaroni & Cheese, NET WT 20 OZ (1 LB 4 OZ) 567g
  • Lot codes: 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
  • Distribution: Nationwide

The hazard

The product contains undeclared soy lecithin, which poses a risk to individuals with soy allergies. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show BEF Foods, Inc. has one other recall on record since May 21, 2019, involving Beef Stroganoff Pasta produced without federal inspection. Other recent recalls of similar products include ASUKAR TETAS Cherry Milkshake Popsicle Recall (March 11, 2026), South Florida Food Cheese Bread Recall (March 9, 2026), and Nutrisystem Chocolate Cheesecake Recall (May 13, 2026).

How to tell if you have this one

Check for the product codes listed in the recall: SUL4839705, SUL4839706, SUL4853771, and other codes listed in the record. The product is sold in 20 oz plastic tubs with paperboard sleeves.

  • Brand
    BEF Foods
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Codes

    Look for the specific product codes listed in the recall: SUL4839705, SUL4839706, SUL4853771, and other codes provided in the record.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Mar 23, 202612. FDA classified it Class II: Jun 10, 202623. Published in FDA’s Enforcement Report: Jun 17, 202634. FDA terminated the recall: Sep 17, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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-0940-2026 (March 23, 2026)
  • Plain-language summary written by qwen3:4b on August 10, 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