FDA recall record
Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10oz bottles; and Electrolit Fruit Punch 6 Pack, 625mL/21 oz; Packaged in a polypropylene bottle with volume capacit...
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 October 1, 2021. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10oz bottles; and Electrolit Fruit Punch 6 Pack, 625mL/21 oz; Packaged in a polypropylene bottle with volume capacity 625 mL and a polypropylene lid and liner with a high-density polyethylene safety ring.
Reason
Product contains undeclared FD&C Red No. 40.
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.
Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10oz bottles; and Electrolit Fruit Punch 6 Pack, 625mL/21 oz; Packaged in a polypropylene bottle with volume capacity 625 mL and a polypropylene lid and liner with a high-density polyethylene safety ring.
Code information listed by FDA
625mL/21oz: Lot #'s: M20D310; M20D311; M20D312; M20D320; M20D327; M20D328; M20D348; M20E306; M20E361; M20E362; M20E363; M20E364; M20F357; M20J308; M20J309; M20J310; M20J311; M20M314; M20M317; M20Y362; M20Y363; M20D324; M20D326; M20D330; M20E305; M20J305; M20J312; M20Y364; M20Y365; M20Y366; M20U341 625mL/21oz Exp.
Dates: 2023-12; 2023-12; 2023-12; 2023-12; 2023-12; 2023-12; 2023-12; 2023-01; 2023-01; 2023-01; 2023-01; 2023-01; 2023-02; 2023-06; 2023-06; 2023-06; 2023-06; 2023-03; 2023-03; 2023-05; 2023-05; 2023-12; 2023-12; 2023-12; 2023-01; 2023-06; 2023-06; 2023-05; 2023-05; 2023-05; 2023-07 300ML/10OZ Lot #'s: H20Y324; H20M130; H20Y328; H20Y361 300ML/10OZ Exp Dates: 2023-05; 2023-03; 2023-05; 2023-05 6 Pack - 625mL/21 oz Lot #'s: M20J304; M20M316 6 Pack - 625mL/21 oz Exp Dates: 2023-06; 2023-03
Distribution and firm information
Recalling firm listed by FDA: Laboratorios Pisa Sa De Cv
Firm location listed by FDA: Guadalajara, N/A, Mexico
Distribution reported by FDA: OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,
Product quantity listed by FDA: 571,590 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.