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Del Monte Foods Inc.
Recall · Class II2018-12-11Terminated

Risk of botulism, a rare but serious kind of poisoning.

Record review found the several productions runs were processed using the incorrect thermal process, and therefore the potential for Clostridium botulinum.

Above, in the agency’s own words. The line before it is our plain-English summary — how we word these.

Issued by the US Food and Drug Administration, naming Del Monte Foods Inc..

What the notice covered

Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g); UPC 0 24000 02770; Ingredient: Vegetables (corn, red and green peppers) water, sea salt. Distributed by Del Monte Foods, Walnut Creek, CA 94598

Quoted from the record as published. If a product is not described here, this notice does not tell us whether it was affected.

What Class II means

The FDA’s middle class: use of the product may cause temporary or medically reversible health consequences, and the probability of serious harm is remote.

This is the agency’s own definition of the class. We do not assign classes and we do not rank them against each other.

The record

Agency
US Food and Drug Administration (FDA)
Reference number
F-0762-2019
Kind of action
Recall
Dated
2018-12-11
Terminated
2019-04-17
Status on the record
Terminated
We read it
2026-10-01

Regulates most packaged food, drugs and devices. Its recall records are published weekly in the Enforcement Report.

Products we matched to this notice

We have not matched this notice to any product in our database — usually because it named no barcode we hold. Products may still have been affected.

How we are treating it

This notice concerns the product line itself or how it was produced.

The government record

The FDA publishes this notice through its enforcement API, so the link below returns raw JSON rather than a readable page. It is the primary record and we cite it as such; everything above is our transcription of it.

https://api.fda.gov/food/enforcement.json?search=recall_number:"F-0762-2019"

To see it in the FDA’s own words, search the reference number F-0762-2019 in the Search the FDA Enforcement Report. The FDA publishes no direct link to an individual recall.

How we source every record on this site