Kuster's Inc. Recall: Kuster's, Inc. is voluntarily recalling its shredded, sliced and cubed cheese following a supplier's recall of cheese due to the potential for the cheese to be contaminated with Listeria monocytogenes or inadequately pasteurized.

🇺🇸 United States

1. October 10, 2016 - Recall initiated
2. December 7, 2016 - Reported by source
3. April 19, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0437-2017

Event ID

75426

Status

Terminated

Classification

Class I

Company

Kuster's Inc.

Product description

Fata's Best Monterey Jack Feather Shred Shredded Cheese, 5 lb. packages packed in plastic bags, keep refrigerated

Quantity

100 lbs.

Reason

Kuster's, Inc. is voluntarily recalling its shredded, sliced and cubed cheese following a supplier's recall of cheese due to the potential for the cheese to be contaminated with Listeria monocytogenes or inadequately pasteurized.

Recall initiation date

October 10, 2016

Report date

December 7, 2016

Classification date

Not published in this source record

Termination date

April 19, 2017

Distribution pattern

Domestic: Michigan, Indiana, Illinois, Ohio,Pennsylvania, South Dakota.

UPC, lot, and code information

lot 27816

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 75426 with 9 other product entries in Public Health Trace.

Responsible company: Kuster's Inc.

Other recalls from Kuster's Inc.

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.

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