Lower riskFood recall · FDA · Published February 26, 2021
Electrolit Fruit Punch Zero: Undeclared Red 40 in 625ml Bottles
Laboratorios Pisa recalls Electrol: 625ml Fruit Punch Zero bottles with undeclared FD&C Red 40. Consumers should check lot numbers M21E366 or M21E367 from January 2024.
“Electrolit Fruit Punch Zero: Undeclared Red 40 in 625ml Bottles.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14834-electrolit-fruit-punch-zero-undeclared-red-40-in-625ml-bottles. Based on FDA recall #F-0364-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0364-2021%22&limit=1).
Laboratorios Pisa Sa De Cv voluntarily recalled Electrolit Fruit Punch Zero beverages on Feb. 26, 2021, after the FDA found undeclared FD&C Red No. 40, according to the FDA.
How to tell if you have it
Brand: Laboratorios Pisa
Product: Electrolit Fruit Punch Zero
Size: 625ML/21OZ
Lot codes: M21E366, M21E367
Expiration dates: 2024-01
Units affected: 571,590 bottles
The hazard
The product contains undeclared FD&C Red No. 40.
Context
GovInfoNow's records show other recent recalls of similar products include Estrella Passion Fruit Drink Recall (2026-05-19) and Rovira Tita Crackers Recall (2025-12-17). Additional similar recalls include Rovira Tempting Crackers Tray Recall (2025-12-17).
How to tell if you have this one
Check for lot numbers M21E366 or M21E367 on the bottle. The product was sold in January 2024 and comes in 625ml polypropylene bottles with a high-density polyethylene safety ring.
Brand
Laboratorios Pisa
Category
Food
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class III
Status
Terminated
Distribution
OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,
Recall number
Product, codes & lots
F-0363-2021
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.; 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
F-0364-2021
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.; Lot #'s: M21E366; M21E367 Exp. Dates: 2024-01; 2024-01
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for lot numbers M21E366 or M21E367 on the bottle label.
Where it went and when
Where it was distributed
Distributed in 22 states.
Listed by the agency
Not listed
FDA distribution: “OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Iowa, Kentucky, Minnesota, Missouri, Nevada, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, Texas, Virginia, Washington, Wisconsin.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class III
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0364-2021 (February 26, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0364-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.