FDA recall record

Kellogg Company Kashi Chewy Trail Mix Granola Bars 1.2 oz individual bar 6 recall — FDA F-1751-2016

Product contains sunflower seeds potentially contaminated with Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and…

Class Iclassification
F-1751-2016official record ID
Jul 27, 2016report date

Recall record at a glance

Official recordF-1751-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmKellogg Company
Report dateJul 27, 2016
Recall initiation dateMay 31, 2016
QuantityN/A
LocationBattle Creek, MI, United States

Official product description

Kashi Chewy Trail Mix Granola Bars 1.2 oz individual bar 6 count retail carton (7.4 oz.), 12 carton per case; 35 count club store carton (42 oz.), 1 carton per case; 12 count food service carton (14.4 oz.), 6 carton per case

Why the product was recalled

Product contains sunflower seeds potentially contaminated with Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.

Distribution information

Nationwide, Canada, Bermuda, Bahamas, Gaum, US Virgin Islands, Mariana Islands

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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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