Check the Batch
Class IITerminated in FDA datasetRecall initiated Jan 8, 2015

JCB FLAVORS, LLC, Product Code 1945 / 2455, Southwestern Seasoning Rub, 9 x 1.36 lb. jar

Recalling firm: JCB Flavors, LLC

Why it was recalled

JCB Flavors is conducting a recall on various Seasonings which used ground cumin as an ingredient received in Oct - Dec 2014. JCB Flavors was informed by their supplier of ground…

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: Jul 5, 2017.

Check your package

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

ProductJCB FLAVORS, LLC, Product Code 1945 / 2455, Southwestern Seasoning Rub, 9 x 1.36 lb. jar, UPC: 851927002895, 851927002901.
Package size1.36 lb
UPC851927002895

FDA code information

Lot Codes: 0822140402, 1028140406 .

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

Full FDA record and distribution details

Original product description

JCB FLAVORS, LLC, Product Code 1945 / 2455, Southwestern Seasoning Rub, 9 x 1.36 lb. jar, UPC: 851927002895, 851927002901.

Extracted codes and context

TypeCode / valueContext
UPC851927002895oduct Code 1945 / 2455, Southwestern Seasoning Rub, 9 x 1.36 lb. jar, UPC: 851927002895, 851927002901.
lot0822140402Lot Codes: 0822140402, 1028140406 .
lot1028140406Lot Codes: 0822140402, 1028140406 .

Original FDA recall reason

JCB Flavors is conducting a recall on various Seasonings which used ground cumin as an ingredient received in Oct - Dec 2014. JCB Flavors was informed by their supplier of ground cumin, Schiff Food Products, that the product tested positive for trace amounts of peanut allergens.

Recall details

Recall number
F-2136-2015
Event ID
70493
FDA status
Terminated
Initiated
Jan 8, 2015
Reported
May 6, 2015
Classified
Apr 29, 2015
Terminated
Jul 5, 2017
Quantity
1040 lbs total from all products
Location
Sullivan, WI, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

WI, IL, MN, CA, IN, NJ, AR.

FDA source record · F-2136-2015

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

Follow official FDA and manufacturer guidance.