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Lower risk Food recall · FDA · Published September 27, 2024

Lunds & Byerlys Lone Star Dip Recall: Potential Mold Contamination

Lunds & Byerlys recalls lone star dip (12 oz) due to potential mold contamination. Products with lot codes 20240826, 20240828, 20240829 and use-by dates up to 10/15/24 may be affected.

🇺🇸 FDA recall #F-0052-2025FoodLunds & Byerlys ›
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Recalling firmLund Food Holdings Inc7752 Mitchell Rd · Eden Prairie, MN 55344-2014
✎ GovInfoNow plain-language explainer

Lunds & Byerlys is recalling lone star dip products that may contain mold. This could cause food poisoning if consumed. Consumers should check the lot code and use-by date on the product. Read more at govinfonow.com/recall/8817-lunds-byerlys-lone-star-dip-recall-potential-mold-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/8817-lunds-byerlys-lone-star-dip-recall-potential-mold-contamination · Updated August 17, 2026 · FDA enforcement record: FDA #F-0052-2025

Cite this page

“Lunds & Byerlys Lone Star Dip Recall: Potential Mold Contamination.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/8817-lunds-byerlys-lone-star-dip-recall-potential-mold-contamination. Based on FDA recall #F-0052-2025 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0052-2025%22&limit=1).

The FDA announced on Sept. 27, 2024, that Lund Food Holdings Inc voluntarily recalled Lunds & Byerlys lone star dip due to potential mold contamination. The recall affects 756 units distributed in Minnesota.

How to tell if you have it

  • Lunds & Byerlys lone star dip
  • Net Wt 12 oz. (340.5g)
  • UPC 0 18169-74197 9
  • Lot Code: 20240826, Use By: 10/15/24
  • Lot Code: 20240828, 20240829, Use By: 10/17/24

The hazard

The product poses a potential mold contamination hazard. The FDA classified the recall as Class II.

Context

GovInfoNow's records show Lund Food Holdings Inc has one other recall on record since Dec. 3, 2025: the Lunds & Byerlys Monster Cookies Recall for undeclared allergens. Other recent recalls of similar products include the Lone Star Dairy Spray Dried Dairy Powder Recall (March 11, 2026), Blackseed Bitters 16oz/32oz Recall (April 6, 2026), and Whole Foods Trio Dip Recall (Aug. 7, 2026).

How to tell if you have this one

Check the lot code on the product label, which should be 20240826, 20240828, or 20240829. The use-by date is listed as October 15, 2024 or October 17, 2024.

  • Brand
    Lunds & Byerlys
  • Product
    Lunds & Byerlys lone star dip. Net Wt 12 oz. (340.5g) UPC 0 18169-74197 9. Produced by Lunds & Byerlys, Edina, MN 55424
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot code (20240826, 20240828, or 20240829) and use-by date (October 15, 2024 or October 17, 2024) on the product.

Where it went and when

Where it was distributed

Distributed in Minnesota.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: 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: “MN” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Minnesota.

Recall timeline

FDA terminated this recall 32 days after the firm started it.

1. Firm started the recall: Sep 27, 202412. FDA classified it Class II: Oct 16, 202423. Published in FDA’s Enforcement Report: Oct 23, 202434. FDA terminated the recall: Oct 29, 202442024
  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 #F-0052-2025 (September 27, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0052-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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