Class IITerminated in FDA datasetRecall initiated May 17, 2012

Thai Seasoning, item number 30502993.01

Recalling firm: Kerry Ingredients & Flavours Research & Developement Center

Why it was recalled

Ingredients used to manufacture seasonings were found to be positive for Salmonella.

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: Nov 15, 2012.

Check your package

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

ProductThai Seasoning, item number 30502993.01 Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 Ingredients: sugar, yeast extract, fructose, garlic powder, salt, maltodextrin, corn starch, modified corn starch, spices, dried red bell pepper, citric acid, vinegar, dextrose, dried red pepper sauce (aged red peppers, vinegar, salt, garlic) sodium deacetate, natural flavor, paprika extract (color), annatto extract (color), and less than 2% silicon dioxide to prevent caking.

FDA code information

Lot code 0507260205

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Full FDA record and distribution details

Original product description

Thai Seasoning, item number 30502993.01 Distributed by Kerry Ingredients & Flavours 3330 Millington Road, Beloit, WI 53511 Ingredients: sugar, yeast extract, fructose, garlic powder, salt, maltodextrin, corn starch, modified corn starch, spices, dried red bell pepper, citric acid, vinegar, dextrose, dried red pepper sauce (aged red peppers, vinegar, salt, garlic) sodium deacetate, natural flavor, paprika extract (color), annatto extract (color), and less than 2% silicon dioxide to prevent caking.

Original FDA recall reason

Ingredients used to manufacture seasonings were found to be positive for Salmonella.

Recall details

Recall number
F-1414-2012
Event ID
61890
FDA status
Terminated
Initiated
May 17, 2012
Reported
Jun 20, 2012
Classified
Jun 13, 2012
Terminated
Nov 15, 2012
Quantity
11 bags (550 pounds)
Location
Beloit, WI, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

AR, IL KS.

FDA source record · F-1414-2012

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

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