Class IITerminated in FDA datasetRecall initiated Jun 5, 2015

CapriSun Variety Pack, with a multi colored plastic wrap with white and yellow lettering,…

Recalling firm: Kraft Foods North America

Why it was recalled

Possible brass fragments in Capri Sun Fruit Punch Flavored Juice Drink Blend.

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: Aug 29, 2016.

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ProductCapriSun Variety Pack, with a multi colored plastic wrap with white and yellow lettering, covering 4 cartons. The 4 cartons consist of fruit punch (the effected product), wild cherry, pacific cooler, and strawberry kiwi.Fruit Punch Flavored Juice Drink Blend in a blue box with white lettering and fruit pictures. The carton contains 10,6 oz pouches.
Package size6 oz

FDA code information

code date: 27 MAY 2016 UPC code for the case: 087684004449 UPC code for the carton of Fruit Punch Flavored Juice Drink Blend: 087684001073

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Full FDA record and distribution details

Original product description

CapriSun Variety Pack, with a multi colored plastic wrap with white and yellow lettering, covering 4 cartons. The 4 cartons consist of fruit punch (the effected product), wild cherry, pacific cooler, and strawberry kiwi.Fruit Punch Flavored Juice Drink Blend in a blue box with white lettering and fruit pictures. The carton contains 10,6 oz pouches.

Original FDA recall reason

Possible brass fragments in Capri Sun Fruit Punch Flavored Juice Drink Blend.

Recall details

Recall number
F-2853-2015
Event ID
71422
FDA status
Terminated
Initiated
Jun 5, 2015
Reported
Jul 22, 2015
Classified
Jul 15, 2015
Terminated
Aug 29, 2016
Quantity
1, 056 cases, 4 cartons per case, 10 pouches per carton.
Location
Granite City, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

The product was distributed to Sams Club Distribution Center, located at 1325 Central Ave, University Park, IL 60484.

FDA source record · F-2853-2015

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

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