FDA recall record

Laboratorios Pisa Sa De Cv Electrolit Fruit Punch Zero, 625ML/21OZ packaged in a recall — FDA F-0364-2021

Product contains undeclared FD&C Red No. 40.

Class IIIclassification
F-0364-2021official record ID
Mar 24, 2021report date

Recall record at a glance

Official recordF-0364-2021
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmLaboratorios Pisa Sa De Cv
Report dateMar 24, 2021
Recall initiation dateFeb 26, 2021
Quantity571,590 bottles
LocationGuadalajara, N/A, Mexico

Official product description

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.

Why the product was recalled

Product contains undeclared FD&C Red No. 40.

Distribution information

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

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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