FDA recall record

Rio Queen Citrus The product was originally distributed in a bulk container of recall — FDA F-1517-2013

Rio Queen Citrus, Inc. of Mission, TX is recalling 840 cartons of 12/1 Dry Pints of Mexican cherry tomatoes in "Karol" brand boxes, because they have the…

Class Iclassification
F-1517-2013official record ID
Jun 19, 2013report date

Recall record at a glance

Official recordF-1517-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmRio Queen Citrus, Inc.
Report dateJun 19, 2013
Recall initiation dateNov 19, 2012
Quantity840 cases (12 pints per case)
LocationMission, TX, United States

Official product description

The product was originally distributed in a bulk container of 12/1 Dry Pints in boxes labeled "Karol" with the Lot No. "01W45" stamped in the upper, right-hand corner on the face of the box. The box states "Distributed by Interstate Fruit & Vegetable", which is an affiliated business of Rio Queen Citrus, Inc. These packages were distributed at the retail level between November 10th & November 19th, 2012. At the retail level, the tomatoes may have been packaged in an alternative container depending on the area and retailer.

Why the product was recalled

Rio Queen Citrus, Inc. of Mission, TX is recalling 840 cartons of 12/1 Dry Pints of Mexican cherry tomatoes in "Karol" brand boxes, because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often e

Distribution information

TX, SC, KS, and Canada

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: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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