FDA recall record
Kool-Aid Jammers Grape packaged in a purple and red box with white lettering.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of February 21, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Kool-Aid Jammers Grape packaged in a purple and red box with white lettering.
Reason
Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Kool-Aid Jammers Grape packaged in a purple and red box with white lettering.
Code information listed by FDA
best when used by code date: 10 DEC 2016 GR02CT762
Distribution and firm information
Recalling firm listed by FDA: Kraft Heinz Foods
Firm location listed by FDA: Northfield, IL, United States
Distribution reported by FDA: The firm distributed the product to 132 domestic firms. Please see the attached spreadsheet for a list of all consignees.
Product quantity listed by FDA: 20, 298 cases, 4 boxes/case, 10 drinks/box.
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.