Great Lakes Cheese Co Inc Recall: 5 lb. loaves of cheese may contain metal foreign material.

🇺🇸 United States

1. October 11, 2019 - Recall initiated
2. December 4, 2019 - Reported by source
3. September 25, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0184-2020

Event ID

84046

Status

Terminated

Classification

Class III

Company

Great Lakes Cheese Co Inc

Product description

Pasteurized Process American Cheese, yellow, 6 - 5lb loaves per case. Brands as follows: 1) Wegmans; 2) Market Basket; 3) Cabot; 4) Field; 5) Foodtown; 6) Hannaford

Quantity

1273 cases

Reason

5 lb. loaves of cheese may contain metal foreign material.

Recall initiation date

October 11, 2019

Report date

December 4, 2019

Classification date

Not published in this source record

Termination date

September 25, 2020

Distribution pattern

Distributed to 12 states: MA, PA, MD, NY, VT, ME, NC, GA, FL, KY, NJ, and IL

UPC, lot, and code information

Expiration Date: 1) 06/23/2020; 2) 06/16/2020; 3) 6/15/2020; 4) 6/22/2020; 5) 6/14/2020, 6/22/2020; 6) 6/14/2020; 6/22/2020

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

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 84046 with 5 other product entries in Public Health Trace.

Responsible company: Great Lakes Cheese Co Inc

Other recalls from Great Lakes Cheese Co Inc

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

Distributed No data published

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
Massachusetts	1
Pennsylvania	1
Maryland	1
New York	1
Vermont	1
Maine	1
North Carolina	1
Georgia	1
Florida	1
Kentucky	1
New Jersey	1
Illinois	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: July 18, 2026 ET

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

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.

• Email
• X / Twitter
• Facebook