Electrolit Ponche/Fruit Punch
Reason Product contains undeclared FD&C Red No. 40.
Electrolit Fruit Punch Zero recall
Recalled by Laboratorios Pisa Sa De Cv · Guadalajara, N/A, Mexico
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Product contains undeclared FD&C Red No. 40.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Electrolit Fruit Punch Zero, 625ML/21OZ packaged in a polypropylene bottle with volume capacity of 625mL and with a polypropylene lid and liner with a high-density polyethylene safety ring.
Quantity: 571,590 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot #'s: M21E366; M21E367 Exp. Dates: 2024-01; 2024-01
Where it was sold
Alabama Arizona California Colorado Florida Georgia Iowa Illinois Indiana Kentucky Minnesota Missouri North Carolina Nevada New York Ohio Oklahoma Pennsylvania Texas Virginia Washington Wisconsin
FDA's distribution note: OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Laboratorios Pisa Sa De Cv
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 26, 2021
- In FDA report of
- Mar 24, 2021
- Terminated
- Oct 1, 2021
- FDA recall number
- F-0364-2021 · event 87441
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.