FDA recall record
BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x6/1 Liter; BODYARMOR SportWater 15/700mL Club; BODYARMOR...
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 June 28, 2023. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x6/1 Liter; BODYARMOR SportWater 15/700mL Club; BODYARMOR SportWater 15/1L Club
Reason
Potential for plastic pieces in product
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.
BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x6/1 Liter; BODYARMOR SportWater 15/700mL Club; BODYARMOR SportWater 15/1L Club
Code information listed by FDA
All codes up to and including BB 021624 UNX LO4
Distribution and firm information
Recalling firm listed by FDA: BA Sports Nutrition, LLC
Firm location listed by FDA: Whitestone, NY, United States
Distribution reported by FDA: IL, KS, SD, OR, WA, MN, UT, AL, IA, TX, AR
Product quantity listed by FDA: approximately 21,000,000 bottles
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.