FDA recall record
Gatorade Combo (Multipack) 24/600 mL
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 September 3, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Gatorade Combo (Multipack) 24/600 mL
Reason
Product is contaminated with mold.
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.
Gatorade Combo (Multipack) 24/600 mL
Code information listed by FDA
(8FP 8O 8LL) 24/600 mL: lot V00762, Exp. Date 7/13/2019 and V00764, Exp. Date 7/12/2019 (8M 8GF 8G) 24/600 mL: lot V00761, Exp. Date 7/14/2019 and lot V00763, Exp. Date 7/3/2019
Distribution and firm information
Recalling firm listed by FDA: The Gatorade Puerto Rico Co
Firm location listed by FDA: Miami, FL, United States
Distribution reported by FDA: Domestic Consignees only. No foreign nor government consignees.
Product quantity listed by FDA: 1,493 cases (24 units per case) 960 for Multipack FP, O and LL and 533 cases for M, GF and G
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.