FDA recall record

Hines Nut Co predominately blue, with a yellow label stating "SALTED JUMBO recall — FDA F-1194-2013

Hines Nut Company Inc. recalled its SALTED JUMBO VIRGINIA IN-SHELL PEANUTS. These peanuts were processed in the Sunland, Inc. Peanut Processing Plant and…

Class Iclassification
F-1194-2013official record ID
Mar 20, 2013report date

Recall record at a glance

Official recordF-1194-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHines Nut Co
Report dateMar 20, 2013
Recall initiation dateOct 15, 2012
QuantityApproximately 57,000 lbs
LocationDallas, TX, United States

Official product description

The HINES package is a cello/poly laminated bag, predominately blue, with a yellow label stating "SALTED JUMBO VIRGINIA PEANUTS" packed as 8 oz, 10 oz, 12 oz, 16 oz and 24 oz; Hines also packages three "theme" cello/poly laminated bags that are 5.5oz each. The themes for these bags are: 1) Independence Day - red, white and blue in color with a stylized flag on the front; 2) Football Season - with a football on the front; and Hunting Season - with a camouflage motif on the front of the bag. The Dollar General Clover Valley package is a cello/poly laminated bag, predominately white with red trim and red lettering. These bags are packaged as 8 oz bags.

Why the product was recalled

Hines Nut Company Inc. recalled its SALTED JUMBO VIRGINIA IN-SHELL PEANUTS. These peanuts were processed in the Sunland, Inc. Peanut Processing Plant and may be contaminated with Salmonella. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and those with weakened immune systems. Healthy persons infected with Salmonella o

Distribution information

Nationwide and Puerto Rico

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

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