Springside Cheese Corp Recall: Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.

🇺🇸 United States

1. February 14, 2018 - Recall initiated
2. March 14, 2018 - Reported by source
3. November 19, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0951-2018

Event ID

79244

Status

Terminated

Classification

Class III

Company

Springside Cheese Corp

Product description

Springside Monterey Jack Caribbean Red Hot Cheese Packaged in the following sizes: Net Wt. 1 lb. and 40 lbs.

Quantity

342.12 lbs.

Reason

Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.

Recall initiation date

February 14, 2018

Report date

March 14, 2018

Classification date

Not published in this source record

Termination date

November 19, 2019

Distribution pattern

AK, CO, FL, IL, MD, NE, SD, TX, WI

UPC, lot, and code information

Lot: 12271703

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

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 79244 with 9 other product entries in Public Health Trace.

Responsible company: Springside Cheese Corp

Other recalls from Springside Cheese Corp

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
Alaska	1
Colorado	1
Florida	1
Illinois	1
Maryland	1
Nebraska	1
South Dakota	1
Texas	1
Wisconsin	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.

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