CLASS I Food recall · Reported 28 Dec 2022 · FDA Enforcement Report
Gamesa Arcoiris Marshmallow Cookies, Naturally recalled
Comercializadora Pepsico Mexico is recalling Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificially Flavored, distributed in California, Texas. The recall was initiated on 7 Nov 2022 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0205-2023
- FDA event ID
- 91135
- Recalling firm
- Comercializadora Pepsico Mexico, Ciudad De Mexico
- Brand
- Gamesa Arcoiris
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 7 Nov 2022
- FDA classified
- 21 Dec 2022
- Reported
- 28 Dec 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Salmonella
- Product category
- Cookies
Timeline
| 7 Nov 2022 | Recall initiated by company | |
| 21 Dec 2022 | Classified by FDA | +44 days |
| 28 Dec 2022 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential to contain Salmonella
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
Gamesa Arcoiris Marshmallow Cookies, Naturally and Artificially Flavored 15.5 Oz, 6 Count UPC 6 86700 10132 4
Where it was distributed
Texas and California
Questions about this recall
Why was it recalled?
Potential to contain Salmonella
Which lots are affected?
Best before 28MAR23 5MY228001 and 28MAR23 6MY128101
Where was it sold?
Texas and California
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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