Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificially Flavored 15.5 Oz, 6 Count UPC 6 86700 10132 4
Summary
The FDA issued a Class I for Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificially Flavored 15.5 Oz by Comercializadora Pepsico Mexico,. Reason: Potential to contain Salmonella.
Details
Source
Food Recall
External ID
F-0205-2023
Action Date
2022-12-28
Status
Terminated
Category
food
Product Description
Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificially Flavored 15.5 Oz, 6 Count UPC 6 86700 10132 4
Lot/Code Info: Best before 28MAR23 5MY228001 and 28MAR23 6MY128101
Quantity Affected: 19,764 boxes
Reason for Recall
Potential to contain Salmonella
Distribution
Texas and California
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-07
Company
Ciudad De Mexico
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 13 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Comercializadora Pepsico Mexico, has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Comercializadora Pepsico Mexico,) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Comercializadora Pepsico Mexico, have FDA actions?
Comercializadora Pepsico Mexico, has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0205-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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