FDA Recall United States Terminated Historical recordClass III
Laboratorios Pisa Sa De Cv
- Product
- Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10o…
- Published
- March 24, 2021
- Distribution
- Multiple states
Laboratorios Pisa Sa De Cv Recall: Product contains undeclared FD&C Red No. 40.
United States
TerminatedClass III
- Company
- Laboratorios Pisa Sa De Cv
- Product
- Electrolit Fruit Punch Zero, 625ML/21OZ packaged in a polypr…
- Recall date
- February 26, 2021
- Terminated
- October 1, 2021
- Source
- FDA
Reason for recall
Product contains undeclared FD&C Red No. 40.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | Not published in this source record | 571,590 bottles | Lot #'s: M21E366; M21E367 Exp. Dates: 2024-01; 2024-01 |
Distribution
- OK
- CA
- WI
- TX
- IN
- IA
- NV
- FL
- NC
- IL
- KY
- OH
- NY
- PA
- AZ
- MO
- AL
- VA
- CO
- WA
- MN
- GA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0364-2021
- Event ID
- 87441
- Status
- Terminated
- Classification
- Class III
- Company
- Laboratorios Pisa Sa De Cv
- 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.
- Quantity
- 571,590 bottles
- Reason
- Product contains undeclared FD&C Red No. 40.
- Recall initiation date
- February 26, 2021
- Report date
- March 24, 2021
- Classification date
- Not published in this source record
- Termination date
- October 1, 2021
- Distribution pattern
- OK, CA, WI, TX, IN, IA, NV, FL, NC, IL, KY, OH, NY, PA, AZ, MO, AL, VA, CO, WA, MN, GA,
- UPC, lot, and code information
- Lot #'s: M21E366; M21E367 Exp. Dates: 2024-01; 2024-01
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 87441 with 1 other product entry in Public Health Trace.
Responsible company: Laboratorios Pisa Sa De Cv
Other recalls from Laboratorios Pisa Sa De Cv
FDA Recall United States Terminated Historical recordClass III
Laboratorios Pisa Sa De Cv
- Product
- Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10o…
- Published
- March 24, 2021
- Distribution
- Multiple states
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Oklahoma | 1 |
| California | 1 |
| Wisconsin | 1 |
| Texas | 1 |
| Indiana | 1 |
| Iowa | 1 |
| Nevada | 1 |
| Florida | 1 |
| North Carolina | 1 |
| Illinois | 1 |
| Kentucky | 1 |
| Ohio | 1 |
| New York | 1 |
| Pennsylvania | 1 |
| Arizona | 1 |
| Missouri | 1 |
| Alabama | 1 |
| Virginia | 1 |
| Colorado | 1 |
| Washington | 1 |
| Minnesota | 1 |
| Georgia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
