CLASS III Food recall · Reported 24 Mar 2021 · FDA Enforcement Report

Electrolit Fruit Punch Zero recalled by Laboratorios Pisa Sa De Cv

Laboratorios Pisa is recalling Electrolit Fruit Punch Zero, distributed in 22 states. The recall was initiated on 26 Feb 2021 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot #'s: M21E366; M21E367 Exp. Dates: 2024-01; 2024-01
Quantity recalled571,590 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0364-2021
FDA event ID
87441
Recalling firm
Laboratorios Pisa, Guadalajara, N/A
Classification
Class III
Status
Terminated
Recall initiated
26 Feb 2021
FDA classified
29 Mar 2021
Reported
24 Mar 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Other

Timeline

26 Feb 2021Recall initiated by company
24 Mar 2021Published in enforcement report+26 days
29 Mar 2021Classified by FDA+5 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains undeclared FD&C Red No. 40.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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.

Where it was distributed

OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,

AlabamaArizonaCaliforniaColoradoFloridaGeorgiaIowaIllinoisIndianaKentuckyMinnesotaMissouriNorth CarolinaNevadaNew YorkOhioOklahomaPennsylvaniaTexasVirginia

Questions about this recall

Why was it recalled?

Product contains undeclared FD&C Red No. 40.

Which lots are affected?

Lot #'s: M21E366; M21E367 Exp. Dates: 2024-01; 2024-01

Where was it sold?

OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 87441
ReportedClassRecallCompanyReasonWhere
CLASS IIIElectrolit Ponche/Fruit Punch recalled by Laboratorios Pisa Sa De CvElectrolit PoncheLaboratorios PisaUndeclared Allergens22 states

More recalls from Laboratorios Pisa

All 2
ReportedClassRecallCompanyReasonWhere
FoodCLASS IIIElectrolit Ponche/Fruit Punch recalled by Laboratorios Pisa Sa De CvElectrolit PoncheLaboratorios PisaUndeclared Allergens22 states

Other Other recalls

All 4,664