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Lower risk Food recall · FDA · Published October 6, 2017

Great Lakes Cheese Co Recalls Shredded Mozzarella Cheese Due to Missing Milk Ingredients

Great Lakes Cheese Co recalls American Accent Shredded Imitation Mozzarella Cheese (UPC 36514-28012) because labeling fails to identify whey or caseinate as milk ingredients. Consumers should check product details and contact the company for more information.

🇺🇸 FDA recall #F-0040-2018FoodGreat Lakes Cheese Co ›
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Contact the company

Recalling firmGreat Lakes Cheese Co Inc17825 Great Lakes Pkwy · Hiram, OH 44234-9677
✎ GovInfoNow plain-language explainer

What happened, in plain English

Great Lakes Cheese Co is recalling American Accent Shredded Imitation Mozzarella Cheese due to labeling that does not identify whey or caseinate as milk ingredients. This means consumers may not know if the product contains milk-derived components, which could affect dietary restrictions. Read more at govinfonow.com/recall/20388-great-lakes-cheese-co-recalls-shredded-mozzarella-cheese-due-to.

Source Summary by GovInfoNow · govinfonow.com/recall/20388-great-lakes-cheese-co-recalls-shredded-mozzarella-cheese-due-to · Updated October 7, 2026 · FDA enforcement record: FDA #F-0040-2018

Cite this page

“Great Lakes Cheese Co Recalls Shredded Mozzarella Cheese Due to Missing Milk Ingredients.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20388-great-lakes-cheese-co-recalls-shredded-mozzarella-cheese-due-to. Based on FDA recall #F-0040-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0040-2018%22&limit=1).

Why it’s dangerous

The product label does not list whey or caseinate as milk ingredients. This could lead to confusion for individuals with dairy allergies or specific dietary needs, as these components are typically derived from milk.

Who’s affected

People with dairy allergies or dietary restrictions who use this cheese product may be affected. Those who rely on clear labeling to avoid milk ingredients are most at risk.

How to tell if you have this one

Check for the UPC 36514-28012 on the label. The product was distributed by Great Lakes Cheese Co. Inc. in Hiram, Ohio and sold with use-by dates from June 2018.

  • Brand
    Great Lakes Cheese Co
  • Product
    American Accent Shredded Imitation Mozzarella Cheese, Net Wt. 32 oz. (2lbs) 907g. UPC 36514-28012 Keep Refrigerated
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 36514-28012 on the label to confirm if the product is recalled.

Where it went and when

Where it was distributed

Distributed in Arizona and New Mexico.

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: 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: yesAZNew Mexico: yesNMKansas: 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: “AZ and NM.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, New Mexico.

Recall timeline

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

1. Firm started the recall: Oct 6, 201712. FDA classified it Class II: Oct 27, 201723. Published in FDA’s Enforcement Report: Nov 8, 201734. FDA terminated the recall: Apr 2, 2018420172018
  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-0040-2018 (October 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0040-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 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