Severity
Low
LowClass IIITerminated
FDA Food recall · Reported March 24, 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.
Product contains undeclared FD&C Red No. 40.
The recall
Laboratorios Pisa Sa De Cv issued this low-severity FDA Food recall — Product contains undeclared FD&C Red No. 40..
- Low
- severity level
- Class III
- classification
- March 24, 2021
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0363-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0363-2021) was formally reported on March 24, 2021, with the manufacturer initiating the action on February 26, 2021. It is classified under Low severity (Class III), with a current status of Terminated. Laboratorios Pisa Sa De Cv is listed as the recalling firm, operating out of Guadalajara, N/A. Federal records list the affected scope as 571,590 bottles.
The documented reason for this recall is: Product contains undeclared FD&C Red No. 40. Distribution data in the federal record shows the product reached: OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category — 22,938 food recalls on record
Where this recall sits in the database
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified low severity.
Affected scope
571,590 bottles
Related Recalls
6
6 from same agency
Product description
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 for recall
Product contains undeclared FD&C Red No. 40.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0363-2021 |
| Date reported | March 24, 2021 |
| Date initiated | February 26, 2021 |
| Recalling firm | Laboratorios Pisa Sa De Cv |
| Firm location | Guadalajara, N/A |
| Affected scope | 571,590 bottles |
| Distribution | OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA, |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Laboratorios Pisa Sa De Cv. Units affected: 571,590 bottles.
Why was this product recalled? ▼
Product contains undeclared FD&C Red No. 40.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on March 24, 2021. Severity: Low. Recall number: F-0363-2021.
Where was the recalled product distributed? ▼
Distribution: OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0363-2021) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported March 24, 2021.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).