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Class ITerminated in FDA datasetRecall initiated Feb 15, 2017

FINLANDIA SRIRACHA JACK & JALAPENO JACK CHEESE NET WT. 12 OZ. (340g) SRIRACHA JACK

Recalling firm: Biery Cheese, Inc.

Why it was recalled

The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 21, 2018.

Check your package

Compare the exact product and package details with the label you have.

ProductFINLANDIA SRIRACHA JACK & JALAPENO JACK CHEESE NET WT. 12 OZ. (340g) SRIRACHA JACK INGREDIENTS: PASTEURIZED MILK, CULTURES, SALT, JALAPENOS, CAYENNE GARLIC, CITRUS POWDER, ENZYMES CONTAINS: MILK JALAPENO JACK INGREDIENTS: PASTEURIZED MILK, RED AND GREEN JALAPENO PEPPERS, CULTURES, SALT, ENZYMES, ANNOTTO CONTAINS: MILK, DISTRIBUTED BY FINLANDIA CHEESE INC., PARSIPPANY, NJ 07054 UPC 6 73803 04508 2
Package size12 OZ
UPC673803045082

FDA code information

Sell By JUL/19/17

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

FINLANDIA SRIRACHA JACK & JALAPENO JACK CHEESE NET WT. 12 OZ. (340g) SRIRACHA JACK INGREDIENTS: PASTEURIZED MILK, CULTURES, SALT, JALAPENOS, CAYENNE GARLIC, CITRUS POWDER, ENZYMES CONTAINS: MILK JALAPENO JACK INGREDIENTS: PASTEURIZED MILK, RED AND GREEN JALAPENO PEPPERS, CULTURES, SALT, ENZYMES, ANNOTTO CONTAINS: MILK, DISTRIBUTED BY FINLANDIA CHEESE INC., PARSIPPANY, NJ 07054 UPC 6 73803 04508 2

Extracted codes and context

TypeCode / valueContext
UPC673803045082 CONTAINS: MILK, DISTRIBUTED BY FINLANDIA CHEESE INC., PARSIPPANY, NJ 07054 UPC 6 73803 04508 2

Original FDA recall reason

The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.

Recall details

Recall number
F-1842-2017
Event ID
76493
FDA status
Terminated
Initiated
Feb 15, 2017
Reported
Apr 12, 2017
Classified
Apr 4, 2017
Terminated
Mar 21, 2018
Quantity
3 cs /15/12 oz packages & 10/12 oz packages
Location
Louisville, OH, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Product was shipped to the following states: FL, GA, IL, IN, KY, MA, MI, NJ, OH, PA & WI.

FDA source record · F-1842-2017

Data updated September 16, 2026. View official FDA data ↗

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