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Great Lakes Cheese Co Inc Recall: Labeling does not identify whey or caseinate as milk ingredients.

United States

TerminatedClass II

Company
Great Lakes Cheese Co Inc
Product
American Accent Shredded Imitation Mozzarella Cheese, Net Wt…
Recall date
October 6, 2017
Terminated
April 2, 2018
Source
FDA

Reason for recall

Labeling does not identify whey or caseinate as milk ingredients.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
American Accent Shredded Imitation Mozzarella Cheese, Net Wt. 32 oz. (2lbs) 907g. UPC 36514-28012 Keep Refrigerated. Distributed by Great Lakes Cheese Co. Inc., Hiram, Ohio 44234. 36514-28012 375 cases (6-2 lb. bags per case) Use By Codes: Jun 8, 2018 S1340P 254 204-1, JUN 22 2018 S1340P 268 204-1, JUN 25 2018 S1340P 271 204-1.

Distribution

  • AZ and NM.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0040-2018
Event ID
78267
Status
Terminated
Classification
Class II
Company
Great Lakes Cheese Co Inc
Product description
American Accent Shredded Imitation Mozzarella Cheese, Net Wt. 32 oz. (2lbs) 907g. UPC 36514-28012 Keep Refrigerated. Distributed by Great Lakes Cheese Co. Inc., Hiram, Ohio 44234.
Quantity
375 cases (6-2 lb. bags per case)
Reason
Labeling does not identify whey or caseinate as milk ingredients.
Recall initiation date
October 6, 2017
Report date
November 8, 2017
Classification date
Not published in this source record
Termination date
April 2, 2018
Distribution pattern
AZ and NM.
UPC, lot, and code information
UPC 36514-28012; Use By Codes: Jun 8, 2018 S1340P 254 204-1, JUN 22 2018 S1340P 268 204-1, JUN 25 2018 S1340P 271 204-1.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Great Lakes Cheese Co Inc

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Distribution
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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Arizona 1
New Mexico 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.