RecallHawk
Class I Recall

Del Monte PB & J Sandwich 6.4 oz UPC 717524770806 packaged in non flexible triangle container

Del Monte Fresh Produce Company

Summary

The FDA issued a Class I for Del Monte PB & J Sandwich 6.4 oz UPC 717524770806 packaged in non flexible trian by Del Monte Fresh Produce Company. Reason: The peanut butter in the snack items have the potential to be contaminated with Salmonella..

Details

Source

Food Recall

External ID

F-1268-2022

Action Date

2022-06-15

Status

Terminated

Category

food

Product Description

Del Monte PB & J Sandwich 6.4 oz UPC 717524770806 packaged in non flexible triangle container

Lot/Code Info: Best If Used By 5/24/2022- 5/30/2022

Quantity Affected: 260 units

Reason for Recall

The peanut butter in the snack items have the potential to be contaminated with Salmonella.

Distribution

FL, IN, PA, TX and OK

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-24

Company

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 197 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Del Monte Fresh Produce Company has 4 FDA actions in our database, including 4 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 (Del Monte Fresh Produce Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Del Monte Fresh Produce Company have FDA actions?

Del Monte Fresh Produce Company has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1268-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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