FDA recall record

Chamberlain Farms Whole Cantaloupe recall — FDA F-2357-2012

Chamberlain Farm Produce, Inc., of Owensville, Indiana, is voluntarily recalling all of its cantaloupes from the 2012 growing season that may remain in…

Class Iclassification
F-2357-2012official record ID
Sep 26, 2012report date

Recall record at a glance

Official recordF-2357-2012
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmChamberlain Farms Inc.
Report dateSep 26, 2012
Recall initiation dateAug 16, 2012
Quantity222,172
LocationOwensville, IN, United States

Official product description

Whole Cantaloupe. Both unlabeled and labeled "MIDWEST BEST" PRODUCE INC. HOMEGROWN CANTALOUPE #4319 PRODUCT OF THE USA

Why the product was recalled

Chamberlain Farm Produce, Inc., of Owensville, Indiana, is voluntarily recalling all of its cantaloupes from the 2012 growing season that may remain in the marketplace. This recall is occurring because of concern some that cantaloupes may be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with

Distribution information

Indiana, Kentucky, Missouri, Illinois, and Iowa with further shipment including Tennessee, Ohio, and Wisconsin. Counties involved include Vanderburgh, Warrick, Gibson, and Dubois County, Indiana, and Wabash County,Illinois.

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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