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Comercializadora Pepsico Mexico, Recall: Potential to contain Salmonella

United States

TerminatedClass I

Company
Comercializadora Pepsico Mexico,
Product
Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificia…
Recall date
November 7, 2022
Terminated
March 24, 2023
Source
FDA

Reason for recall

Potential to contain Salmonella

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificially Flavored 15.5 Oz, 6 Count UPC 6 86700 10132 4 Not published in this source record 19,764 boxes Best before 28MAR23 5MY228001 and 28MAR23 6MY128101

Distribution

  • Texas and California

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0205-2023
Event ID
91135
Status
Terminated
Classification
Class I
Company
Comercializadora Pepsico Mexico,
Product description
Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificially Flavored 15.5 Oz, 6 Count UPC 6 86700 10132 4
Quantity
19,764 boxes
Reason
Potential to contain Salmonella
Recall initiation date
November 7, 2022
Report date
December 28, 2022
Classification date
Not published in this source record
Termination date
March 24, 2023
Distribution pattern
Texas and California
UPC, lot, and code information
Best before 28MAR23 5MY228001 and 28MAR23 6MY128101
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Comercializadora Pepsico Mexico,

Other recalls from Comercializadora Pepsico Mexico,

FDA Recall United States Terminated Historical recordClass I

Comercializadora Pepsico Mexico,

Product
QUAKER PANCAKES WITH WHOLE GRAIN OATS, NET WT 15.97OZ (1LB)
Published
October 18, 2023
Distribution
Puerto Rico, Dominican Republic

View recall →

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.