FDA recall record

Kraft Foods CapriSun Pack, with a multi colored plastic wrap with white recall — FDA F-2853-2015

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

Class IIclassification
F-2853-2015official record ID
Jul 22, 2015report date

Recall record at a glance

Official recordF-2853-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKraft Foods North America
Report dateJul 22, 2015
Recall initiation dateJun 5, 2015
Quantity1, 056 cases, 4 cartons per case, 10 pouches per carton.
LocationGranite City, IL, United States

Official 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.

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.