RecallHawk
Class I Recall

FG21002 Potato, Cooked Breakfast 2514111; 2514111B FG21002 Potato, Cooked Breakfast 2514311 Packaged 3- 5 lb poly

AND GO CONCEPTS DBA SALAD AND GO

Summary

The FDA issued a Class I for FG21002 Potato, Cooked Breakfast 2514111; 2514111B FG21002 Potato, Cooked Br by AND GO CONCEPTS DBA SALAD AND GO. Reason: Potential to be contaminated with Listeria monocytogenes.

Details

Source

Food Recall

External ID

H-0269-2025

Action Date

2025-07-23

Status

Terminated

Category

food

Product Description

FG21002 Potato, Cooked Breakfast 2514111; 2514111B FG21002 Potato, Cooked Breakfast 2514311 Packaged 3- 5 lb polybags per cardboard case

Lot/Code Info: 2514111; 2514111B; 2514311

Quantity Affected: 98 cases; 296 bags

Reason for Recall

Potential to be contaminated with Listeria monocytogenes

Distribution

Arizona and Nevada

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-27

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

AND GO CONCEPTS DBA SALAD AND GO has 12 FDA actions in our database, including 12 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 (AND GO CONCEPTS DBA SALAD AND GO) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does AND GO CONCEPTS DBA SALAD AND GO have FDA actions?

AND GO CONCEPTS DBA SALAD AND GO has 12 FDA actions in our database, including 12 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0269-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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